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Furosemide

Prescription ANDA TE AB Official labelling
Informational index, not medical advice. Content is reproduced from public FDA and NLM data. Always confirm against the manufacturer's current prescribing information. Report adverse events to FDA MedWatch.

Overview

Brand name
Furosemide
Generic name
Furosemide
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA
Labeler
A-S Medication Solutions
Product type
Human Prescription Drug
DEA schedule
Not scheduled
Active ingredients
3
NDC product codes
126
Packages
352
Data completeness
83% of corroborating sources present

Active ingredients

Source: NDC Directory
Active ingredients and strengths as listed in the NDC Directory.
Ingredient Strength RxCUI Monograph
Furosemide 20 mg/1 1719291 View
Furosemide 40 mg/1 1719291 View
Furosemide 80 mg/1 1719291 View

Forms, strengths and routes

Source: NDC Directory
Dosage form
Tablet
Route of administration
Oral
Presentations
400

Pharmacologic classes are listed in the class section below.

Pharmacologic class

Source: NDC Directory
Established pharmacologic classes (EPC), mechanisms of action (MoA), chemical structures (CS) and physiologic effects (PE).
Class Type Browse
Increased Diuresis at Loop of Henle [PE] PE All 12 members
Loop Diuretic [EPC] EPC All 12 members

Regulatory status

Source: Drugs@FDANDC Directory
Application number
076796
Application type
ANDA · Abbreviated New Drug Application
Approval date
March 26, 2004
Sponsor
PRINSTON INC
Products on application
3
Submissions recorded
8
Products approved under application 076796.
Product Trade name Form Strength Ingredient Status TE Flags
076796-001 FUROSEMIDE TABLET FUROSEMIDE Prescription AB
076796-002 FUROSEMIDE TABLET FUROSEMIDE Prescription AB
076796-003 FUROSEMIDE TABLET FUROSEMIDE Prescription AB

Therapeutic equivalence

Source: Orange Book
TE code
AB
Reference Listed Drug
No
Reference Standard
No

What this rating means: Therapeutically equivalent — bioequivalence demonstrated by in vivo or in vitro testing

Codes beginning with “A” indicate products the FDA considers therapeutically equivalent. Codes beginning with “B” indicate bioequivalence has not been established. See methodology.

Approval history

Source: Drugs@FDA
Most recent submissions on application 076796.
Type No. Action Status Date Review
Supplement 20 Labeling Approved May 31, 2020 Standard
Supplement 16 Labeling Approved May 31, 2020 Standard
Supplement 11 Labeling Approved May 9, 2012 Standard
Supplement 9 Labeling Approved January 27, 2011 —
Supplement 5 Labeling Approved February 20, 2009 —
Supplement 4 Labeling Approved August 9, 2007 —
Supplement 2 Labeling Approved May 1, 2006 —
Original application 1 Approved March 26, 2004 —

Prescribing information

Source: openFDA Drug Labeling

Reproduced verbatim from the Structured Product Labeling submitted to the FDA (effective 20260429). This is the manufacturer's labelling text, not a summary and not advice.

HUMAN PRESCRIPTION DRUG · 20260429 HUMAN PRESCRIPTION DRUG · 20260101 HUMAN PRESCRIPTION DRUG · 20251224 HUMAN PRESCRIPTION DRUG · 20241226

Indications and Usage

openFDA Drug Labeling

INDICATIONS AND USAGE Edema Furosemide tablets are indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome. Furosemide tablets are particularly useful when an agent with greater diuretic potential is desired. Hypertension Oral furosemide may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents. Hypertensive patients who cannot be adequately controlled with thiazides will probably also not be adequately controlled with furosemide alone.

Edema Furosemide tablets are indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome. Furosemide tablets are particularly useful when an agent with greater diuretic potential is desired.

Hypertension Oral furosemide may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents. Hypertensive patients who cannot be adequately controlled with thiazides will probably also not be adequately controlled with furosemide alone.

Dosage and Administration

openFDA Drug Labeling

DOSAGE AND ADMINISTRATION Edema Therapy should be individualized according to patient response to gain maximal therapeutic response and to determine the minimal dose needed to maintain that response. Adults - The usual initial dose of furosemide tablets is 20 to 80 mg given as a single dose. Ordinarily a prompt diuresis ensues. If needed, the same dose can be administered 6 to 8 hours later or the dose may be increased. The dose may be raised by 20 or 40 mg and given not sooner than 6 to 8 hours after the previous dose until the desired diuretic effect has been obtained. The individually determined single dose should then be given once or twice daily (e.g., at 8 am and 2 pm). The dose of furosemide tablets may be carefully titrated up to 600 mg/day in patients with clinically severe edematous states. Edema may be most efficiently and safely mobilized by giving furosemide tablets on 2 to 4 consecutive days each week. When doses exceeding 80 mg/day are given for prolonged periods, careful clinical observation and laboratory monitoring are particularly advisable (see PRECAUTIONS: Laboratory Tests ). Geriatric Patients - In general, dose selection for the elderly patient should be cautious, usually starting at the low end of the dosing range (see PRECAUTIONS: Geriatric Use ). Pediatric Patients - The usual initial dose of oral furosemide in pediatric patients is 2 mg/kg body weight, given as a single dose. If the diuretic response is not satisfactory after the initial dose, dosage may be increased by 1 or 2 mg/kg no sooner than 6 to 8 hours after the previous dose. Doses greater than 6 mg/kg body weight are not recommended. For maintenance therapy in pediatric patients, the dose should be adjusted to the minimum effective level. Hypertension Therapy should be individualized according to the patient's response to gain maximal therapeutic response and to determine the minimal dose needed to maintain the therapeutic response. Adults - The usual initial dose of furosemide tablets for hypertension is 80 mg, usually divided into 40 mg twice a day. Dosage should then be adjusted according to response. If response is not satisfactory, add other antihypertensive agents. Changes in blood pressure must be carefully monitored when furosemide tablets are used with other antihypertensive drugs, especially during initial therapy. To prevent excessive drop in blood pressure, the dosage of other agents should be reduced by at least 50 percent when furosemide tablets are added to the regimen. As the blood pressure falls under the potentiating effect of furosemide tablets, a further reduction in dosage or even discontinuation of other antihypertensive drugs may be necessary. Geriatric Patients - In general, dose selection and dose adjustment for the elderly patient should be cautious, usually starting at the low end of the dosing range (see PRECAUTIONS: Geriatric Use ).

Edema Therapy should be individualized according to patient response to gain maximal therapeutic response and to determine the minimal dose needed to maintain that response. Adults - The usual initial dose of furosemide tablets is 20 to 80 mg given as a single dose. Ordinarily a prompt diuresis ensues. If needed, the same dose can be administered 6 to 8 hours later or the dose may be increased. The dose may be raised by 20 or 40 mg and given not sooner than 6 to 8 hours after the previous dose until the desired diuretic effect has been obtained. The individually determined single dose should then be given once or twice daily (e.g., at 8 am and 2 pm). The dose of furosemide tablets may be carefully titrated up to 600 mg/day in patients with clinically severe edematous states. Edema may be most efficiently and safely mobilized by giving furosemide tablets on 2 to 4 consecutive days each week. When doses exceeding 80 mg/day are given for prolonged periods, careful clinical observation and laboratory monitoring are particularly advisable (see PRECAUTIONS: Laboratory Tests ). Geriatric P …

Contraindications

openFDA Drug Labeling

CONTRAINDICATIONS Furosemide tablets are contraindicated in patients with anuria and in patients with a history of hypersensitivity to furosemide.

Warnings and Cautions

openFDA Drug Labeling

WARNINGS In patients with hepatic cirrhosis and ascites, furosemide therapy is best initiated in the hospital. In hepatic coma and in states of electrolyte depletion, therapy should not be instituted until the basic condition is improved. Sudden alterations of fluid and electrolyte balance in patients with cirrhosis may precipitate hepatic coma; therefore, strict observation is necessary during the period of diuresis. Supplemental potassium chloride and, if required, an aldosterone antagonist are helpful in preventing hypokalemia and metabolic alkalosis. If increasing azotemia and oliguria occur during treatment of severe progressive renal disease, furosemide should be discontinued. Cases of tinnitus and reversible or irreversible hearing impairment and deafness have been reported. Reports usually indicate that furosemide ototoxicity is associated with rapid injection, severe renal impairment, the use of higher than recommended doses, hypoproteinemia or concomitant therapy with aminoglycoside antibiotics, ethacrynic acid, or other ototoxic drugs. If the physician elects to use high dose parenteral therapy, controlled intravenous infusion is advisable (for adults, an infusion rate not exceeding 4mg furosemide per minute has been used) (see PRECAUTIONS : Drug Interactions).

WARNINGS SECTION Furosemide is a potent diuretic which, if given in excessive amounts, can lead to a profound diuresis with water and electrolyte depletion. Therefore, careful medical supervision is required and dose and dose schedule must be adjusted to the individual patient's needs (see DOSAGE AND ADMINISTRATION ).

WARNINGS SECTION In patients with hepatic cirrhosis and ascites, furosemide therapy is best initiated in the hospital. In hepatic coma and in states of electrolyte depletion, therapy should not be instituted until the basic condition is improved. Sudden alterations of fluid and electrolyte balance in patients with cirrhosis may precipitate hepatic coma; therefore, strict observation is necessary during the period of diuresis. Supplemental potassium chloride and, if required, an aldosterone antagonist are helpful in preventing hypokalemia and metabolic alkalosis. If increasing azotemia and oliguria occur during treatment of severe progressive renal disease, furosemide should be discontinued. Cases of tinnitus and reversible or irreversible hearing impairment and deafness have been reported. Reports usually indicate that furosemide ototoxicity is associated with rapid injection, severe renal impairment, the use of higher than recommended doses, hypoproteinemia or concomitant therapy with aminoglycoside antibiotics, ethacrynic acid, or other ototoxic drugs. If the physician elects to use high dose parenteral therapy, controlled intravenous infusion is advisable (for adults, an infusion rate not exceeding 4 mg furosemide per minute has been used) (see PRECAUTIONS: Drug Interactions ).

Adverse Reactions

openFDA Drug Labeling

ADVERSE REACTIONS Adverse reactions are categorized below by organ system and listed by decreasing severity. Gastrointestinal System Reactions 1. hepatic encephalopathy in patients with hepato-cellular insufficiency 2. pancreatitis 3. jaundice (intrahepatic cholestatic jaundice) 4. increased liver enzymes 5. anorexia 6. oral and gastric irritation 7. cramping 8. diarrhea 9. constipation 10. nausea 11. vomiting Systemic Hypersensitivity Reactions 1. Severe anaphylactic or anaphylactoid reactions (e.g. with shock) 2. systemic vasculitis 3. interstitial nephritis 4. necrotizing angiitis Central Nervous System Reactions 1. tinnitus and hearing loss 2. paresthesias 3. vertigo 4. dizziness 5. headache 6. blurred vision 7. xanthopsia Hematologic Reactions 1. aplastic anemia 2. thrombocytopenia 3. agranulocytosis 4. hemolytic anemia 5. leukopenia 6. anemia 7. eosinophilia Dermatologic-Hypersensitivity Reactions 1. toxic epidermal necrolysis 2. Stevens-Johnson Syndrome 3. erythema multiforme 4. drug rash with eosinophilia and systemic symptoms 5. acute generalized exanthematous pustulosis 6. exfoliative dermatitis 7. bullous pemphigoid 8. purpura 9. photosensitivity 10. rash 11. pruritis 12. urticaria Cardiovascular Reaction 1. Orthostatic hypotension may occur and be aggravated by alcohol, barbiturates or narcotics. 2. Increase in cholesterol and triglyceride serum levels Other Reactions 1. hyperglycemia 2. glycosuria 3. hyperuricemia 4. muscle spasm 5. weakness 6. restlessness 7. urinary bladder spasm 8. thrombophlebitis 9. fever Whenever adverse reactions are moderate or severe, Furosemide tablets dosage should be reduced or therapy withdrawn. CALL YOUR DOCTOR FOR MEDICAL ADVICE ABOUT SIDE EFFECTS. YOU MAY REPORT SIDE EFFECTS TO THE FDA AT 1-800-FDA-1088 OR LEADING PHARMA, LLC AT 1-844-740-7500.

Drug Interactions

openFDA Drug Labeling

Drug Interactions Furosemide tablets may increase the ototoxic potential of aminoglycoside antibiotics, especially in the presence of impaired renal function. Except in life-threatening situations, avoid this combination. Furosemide tablets should not be used concomitantly with ethacrynic acid because of the possibility of ototoxicity. Patients receiving high doses of salicylates concomitantly with Furosemide tablets, as in rheumatic disease, may experience salicylate toxicity at lower doses because of competitive renal excretory sites. There is a risk of ototoxic effects if cisplatin and Furosemide tablets are given concomitantly. In addition, nephrotoxicity of nephrotoxic drugs such as cisplatin may be enhanced if Furosemide tablets are not given in lower doses and with positive fluid balance when used to achieve forced diuresis during cisplatin treatment. Furosemide tablets have a tendency to antagonize the skeletal muscle relaxing effect of tubocurarine and may potentiate the action of succinylcholine. Lithium generally should not be given with diuretics because they reduce lithium’s renal clearance and add a high risk of lithium toxicity. Furosemide tablets combined with angiotensin converting enzyme inhibitors or angiotensin II receptor blockers may lead to severe hypotension and deterioration in renal function, including renal failure. An interruption or reduction in the dosage of Furosemide tablets, angiotensin converting enzyme inhibitors, or angiotensin receptor blockers may be necessary. Potentiation occurs with ganglionic or peripheral adrenergic blocking drugs. Furosemide tablets may decrease arterial responsiveness to norepinephrine. However, norepinephrine may still be used effectively. Simultaneous administration of sucralfate and Furosemide tablets may reduce the natriuretic and antihypertensive effects of Furosemide tablets. Patients receiving both drugs should be observed closely to determine if the desired diuretic and/or antihypertensive effect of Furosemide tablets is achieved. The intake of Furosemide tablets and sucralfate should be separated by at least two hours. In isolated cases, intravenous administration of Furosemide tablets within 24 hours of taking chloral hydrate may lead to flushing, sweating attacks, restlessness, nausea, increase in blood pressure, and tachycardia. Use of Furosemide tablets concomitantly with chloral hydrate is, therefore, not recommended. Phenytoin interferes directly with renal action of Furosemide tablets. There is evidence that treatment with phenytoin leads to decrease intestinal absorption of Furosemide tablets, and consequently to lower peak serum furosemide concentrations. Methotrexate and other drugs that, like Furosemide tablets, undergo significant renal tubular secretion may reduce the effect of Furosemide tablets. Conversely, Furosemide tablets may decrease renal elimination of other drugs that undergo tubular secretion. High-dose treatment of both Furosemide tablets and these other drugs may result in elevated serum levels of these drugs and may potentiate their toxicity as well as the toxicity of Furosemide tablets. Furosemide tablets can increase the risk of cephalosporin-induced nephrotoxicity even in the setting of minor or transient renal impairment. Concomitant use of cyclosporine and Furosemide tablets is associated with increased risk of gouty arthritis secondary to Furosemide tablets-induced hyperurecemia and cyclosporine impairment of renal urate excretion. High doses (>80mg) of furosemide may inhibit the binding of thyroid hormones to carrier proteins and result in transient increase in free thyroid hormones, followed by an overall decrease in total thyroid hormone levels. One study in six subjects demonstrated that the combination of furosemide and acetylsalicylic acid temporarily reduced creatinine clearance in patients with chronic renal insufficiency. There are case reports of patients who developed increased BUN, serum creatinine and serum pota …

Description

openFDA Drug Labeling

DESCRIPTION Each tablet for oral administration contains: Furosemide, USP . . . . . . . . . . . . . . . . 20 mg, 40 mg and 80 mg Each mL of Oral Solution for oral administration contains: Furosemide, USP . . . . . . . . . . . . . . . . 10 mg per mL or 8 mg (40 mg per 5 mL) Furosemide is a diuretic which is an anthranilic acid derivative. Chemically, it is 4-chloro- N -furfuryl-5-sulfamoylanthranilic acid. Furosemide is a white to slightly yellow, crystalline powder. It is practically insoluble in water; freely soluble in acetone, dimethylformamide and in solutions of alkali hydroxides; soluble in methanol; sparingly soluble in alcohol; slightly soluble in ether; very slightly soluble in chloroform. The CAS Registry Number is 54-31-9. The structural formula is as follows: C 12 H 11 ClN 2 O 5 S M.W. 330.74 Furosemide Tablets, USP are available for oral administration containing 20 mg, 40 mg or 80 mg of Furosemide, USP. The tablets meet Dissolution Test 1. Each tablet contains the following inactive ingredients: colloidal silicon dioxide, corn starch, lactose monohydrate, microcrystalline cellulose, pregelatinized starch, purified water, sodium lauryl sulfate, sodium starch glycolate and stearic acid. Furosemide Oral Solution, USP is also available for oral administration containing either 10 mg per mL or 40 mg per 5 mL. The oral solution contains the following inactive ingredients: D and C Yellow No. 10, FD and C Yellow No. 6, flavors, potassium carbonate 11⁄2 hydrate, propylene glycol, purified water and sorbitol solution. The 10 mg/mL solution is orange flavored and contains prosweet liquid and saccharin sodium. The 40 mg/5 mL solution is pineapple-peach flavored and contains sweet tone. furosemide structural formula image

OVERDOSAGE The principal signs and symptoms of overdose with FUROSEMIDE TABLET are dehydration, blood volume reduction, hypotension, electrolyte imbalance, hypokalemia and hypochloremic alkalosis, and are extensions of its diuretic action. The acute toxicity of FUROSEMIDE TABLET has been determined in mice, rats and dogs. In all three, the oral LD 50 exceeded 1000 mg/kg body weight, while the intravenous LD 50 ranged from 300 to 680 mg/kg. The acute intragastric toxicity in neonatal rats is 7 to 10 times that of adult rats. The concentration of FUROSEMIDE TABLET in biological fluids associated with toxicity or death is not known. Treatment of overdosage is supportive and consists of replacement of excessive fluid and electrolyte losses. Serum electrolytes, carbon dioxide level and blood pressure should be determined frequently. Adequate drainage must be assured in patients with urinary bladder outlet obstruction (such as prostatic hypertrophy). Hemodialysis does not accelerate furosemide elimination.

How Supplied / Storage and Handling

openFDA Drug Labeling

HOW SUPPLIED Furosemide Tablets USP 20 mg tablets are supplied as white, flat tablets with beveled edges, product identification “54 840” debossed on one side. NDC 0054-8297-25: Unit dose amber blisters, 10 Tablets per strip, 10 strips per shelf pack, 10 shelf packs per shipper NDC 0054-4297-25: Bottle of 100 Tablets NDC 0054-4297-31: Bottle of 1000 Tablets 40 mg tablets are supplied as white, flat tablets with beveled edges, scored on one side and product identification “54 583” debossed on one side. NDC 0054-8299-25: Unit dose amber blisters, 10 Tablets per strip, 10 strips per shelf pack, 10 shelf packs per shipper NDC 0054-4299-25: Bottle of 100 Tablets NDC 0054-4299-31: Bottle of 1000 Tablets 80 mg tablets are supplied as white, flat tablets with beveled edges, scored on one side and product identification “54 533” debossed on one side. NDC 0054-8301-25: Unit dose amber blisters, 10 Tablets per strip, 10 strips per shelf pack, 10 shelf packs per shipper NDC 0054-4301-25: Bottle of 100 Tablets NDC 0054-4301-29: Bottle of 500 Tablets Store and Dispense Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature.] Note: Dispense in a tight, light-resistant, child-resistant container as defined in the USP/NF. Exposure to light may cause slight discoloration. Discolored tablets should not be dispensed. Protect From Moisture. PROTECT FROM LIGHT. Furosemide Oral Solution USP 10 mg per mL oral solution is supplied as a (orange-flavored) clear, orange-colored solution. NDC 0054-3294-46: Bottle of 60 mL Dispense only in this bottle and only with the calibrated dropper provided. NDC 0054-3294-50: Bottle of 120 mL Dispense only in this bottle. PROTECT FROM LIGHT. NOTE: DISCARD OPENED BOTTLE AFTER 90 DAYS. 40 mg per 5 mL oral solution is supplied as a (pineapple-peach flavored) clear, orange-colored solution. NDC 0054-3298-63: Bottle of 500 mL Dispense in a tight, light-resistant, child-resistant container as defined in the USP/NF. PROTECT FROM LIGHT. Store and Dispense Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature.] Distr. by: West-Ward Pharmaceuticals Corp. Eatontown, NJ 07724 4052002//11 Revised January 2016

Adverse event reports

Source: openFDA FAERS
398,368
FAERS reports mentioning this drug
as of 2026-09-25T03:42:24+00:00
A report count is not a risk measure. FAERS accepts voluntary and mandatory reports without establishing causation, and reporting is influenced by how widely a drug is used, how long it has been marketed, and media attention. FDA states that reports “do not prove that the drug caused the event”. Compare rates, not totals.

Attributed to this product's most-reported active ingredient: FUROSEMIDE. Combination products with more than six active ingredients are not attributed, because a report count summed across a long ingredient list measures the list, not the medicine.

Recalls

Source: FDA Enforcement
Drug recall enforcement reports associated with this product.
Classification Reported Firm Reason Status
Class II April 29, 2026 Leading Pharma, LLC CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit. Ongoing
Class II January 28, 2026 Graviti Pharmaceuticals Private Limited Presence of Foreign Substance Ongoing

Packaging and NDCs

Source: NDC Directory showing the first 400
Every National Drug Code package associated with this medication. The NDC is the identifier used for dispensing, billing and pharmacovigilance in the United States.
Package NDC Product NDC Labeler Description Marketing start
50090-2713-0 50090-2713 A-S Medication Solutions 100 TABLET in 1 BOTTLE (50090-2713-0) December 14, 2016
50090-3313-0 50090-3313 A-S Medication Solutions 30 TABLET in 1 BOTTLE (50090-3313-0) September 23, 2021
50090-3313-1 50090-3313 A-S Medication Solutions 100 TABLET in 1 BOTTLE (50090-3313-1) January 2, 2018
50090-3313-3 50090-3313 A-S Medication Solutions 60 TABLET in 1 BOTTLE (50090-3313-3) January 12, 2022
50090-3313-9 50090-3313 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-3313-9) December 27, 2017
50090-5429-0 50090-5429 A-S Medication Solutions 30 TABLET in 1 BOTTLE (50090-5429-0) January 11, 2021
50090-5429-1 50090-5429 A-S Medication Solutions 100 TABLET in 1 BOTTLE (50090-5429-1) January 11, 2021
50090-5429-7 50090-5429 A-S Medication Solutions 200 TABLET in 1 BOTTLE (50090-5429-7) January 17, 2023
50090-5429-8 50090-5429 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-5429-8) January 11, 2021
50090-5702-0 50090-5702 A-S Medication Solutions 100 TABLET in 1 BOTTLE (50090-5702-0) September 23, 2021
50090-5702-1 50090-5702 A-S Medication Solutions 180 TABLET in 1 BOTTLE (50090-5702-1) April 18, 2023
50090-6219-0 50090-6219 A-S Medication Solutions 30 TABLET in 1 BOTTLE (50090-6219-0) November 10, 2022
50090-6219-1 50090-6219 A-S Medication Solutions 100 TABLET in 1 BOTTLE (50090-6219-1) November 10, 2022
50090-6219-7 50090-6219 A-S Medication Solutions 200 TABLET in 1 BOTTLE (50090-6219-7) November 10, 2022
50090-6219-8 50090-6219 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-6219-8) November 10, 2022
50090-6642-0 50090-6642 A-S Medication Solutions 30 TABLET in 1 BOTTLE (50090-6642-0) August 29, 2023
50090-6642-1 50090-6642 A-S Medication Solutions 100 TABLET in 1 BOTTLE (50090-6642-1) August 29, 2023
50090-6642-8 50090-6642 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-6642-8) August 29, 2023
50090-6646-0 50090-6646 A-S Medication Solutions 30 TABLET in 1 BOTTLE (50090-6646-0) August 29, 2023
50090-6646-1 50090-6646 A-S Medication Solutions 100 TABLET in 1 BOTTLE (50090-6646-1) August 29, 2023
50090-6646-3 50090-6646 A-S Medication Solutions 60 TABLET in 1 BOTTLE (50090-6646-3) August 29, 2023
50090-6646-9 50090-6646 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-6646-9) August 29, 2023
50090-6647-1 50090-6647 A-S Medication Solutions 180 TABLET in 1 BOTTLE (50090-6647-1) August 29, 2023
50090-6937-0 50090-6937 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-6937-0) December 15, 2023
50090-6942-0 50090-6942 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-6942-0) December 15, 2023
50090-7703-0 50090-7703 A-S Medication Solutions 30 TABLET in 1 BOTTLE (50090-7703-0) October 14, 2025
50090-7703-1 50090-7703 A-S Medication Solutions 100 TABLET in 1 BOTTLE (50090-7703-1) October 14, 2025
50090-7703-3 50090-7703 A-S Medication Solutions 60 TABLET in 1 BOTTLE (50090-7703-3) October 14, 2025
50090-7703-9 50090-7703 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-7703-9) October 14, 2025
50090-7704-1 50090-7704 A-S Medication Solutions 180 TABLET in 1 BOTTLE (50090-7704-1) October 14, 2025
50090-7705-0 50090-7705 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-7705-0) October 14, 2025
50090-7706-0 50090-7706 A-S Medication Solutions 30 TABLET in 1 BOTTLE (50090-7706-0) October 14, 2025
50090-7706-1 50090-7706 A-S Medication Solutions 100 TABLET in 1 BOTTLE (50090-7706-1) October 14, 2025
50090-7706-7 50090-7706 A-S Medication Solutions 200 TABLET in 1 BOTTLE (50090-7706-7) October 14, 2025
50090-7706-8 50090-7706 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-7706-8) October 14, 2025
50090-7708-0 50090-7708 A-S Medication Solutions 90 TABLET in 1 BOTTLE (50090-7708-0) October 14, 2025
43353-069-30 43353-069 Aphena Pharma Solutions - Tennessee, LLC 30 TABLET in 1 BOTTLE (43353-069-30) June 19, 2017
43353-069-45 43353-069 Aphena Pharma Solutions - Tennessee, LLC 45 TABLET in 1 BOTTLE (43353-069-45) June 19, 2017
43353-069-53 43353-069 Aphena Pharma Solutions - Tennessee, LLC 60 TABLET in 1 BOTTLE (43353-069-53) June 19, 2017
43353-069-60 43353-069 Aphena Pharma Solutions - Tennessee, LLC 90 TABLET in 1 BOTTLE (43353-069-60) June 19, 2017
43353-069-80 43353-069 Aphena Pharma Solutions - Tennessee, LLC 180 TABLET in 1 BOTTLE (43353-069-80) June 19, 2017
43353-747-30 43353-747 Aphena Pharma Solutions - Tennessee, LLC 30 TABLET in 1 BOTTLE, PLASTIC (43353-747-30) May 1, 2017
43353-747-45 43353-747 Aphena Pharma Solutions - Tennessee, LLC 45 TABLET in 1 BOTTLE, PLASTIC (43353-747-45) August 22, 2017
43353-747-53 43353-747 Aphena Pharma Solutions - Tennessee, LLC 60 TABLET in 1 BOTTLE, PLASTIC (43353-747-53) May 1, 2017
43353-747-60 43353-747 Aphena Pharma Solutions - Tennessee, LLC 90 TABLET in 1 BOTTLE, PLASTIC (43353-747-60) August 2, 2011
43353-747-80 43353-747 Aphena Pharma Solutions - Tennessee, LLC 180 TABLET in 1 BOTTLE, PLASTIC (43353-747-80) May 1, 2017
43353-747-92 43353-747 Aphena Pharma Solutions - Tennessee, LLC 270 TABLET in 1 BOTTLE, PLASTIC (43353-747-92) August 22, 2017
71610-049-30 71610-049 Aphena Pharma Solutions - Tennessee, LLC 30 TABLET in 1 BOTTLE, PLASTIC (71610-049-30) April 16, 2018
71610-049-45 71610-049 Aphena Pharma Solutions - Tennessee, LLC 45 TABLET in 1 BOTTLE, PLASTIC (71610-049-45) April 16, 2018
71610-049-53 71610-049 Aphena Pharma Solutions - Tennessee, LLC 60 TABLET in 1 BOTTLE, PLASTIC (71610-049-53) April 16, 2018
71610-049-60 71610-049 Aphena Pharma Solutions - Tennessee, LLC 90 TABLET in 1 BOTTLE, PLASTIC (71610-049-60) April 16, 2018
71610-049-80 71610-049 Aphena Pharma Solutions - Tennessee, LLC 180 TABLET in 1 BOTTLE, PLASTIC (71610-049-80) April 16, 2018
71610-096-30 71610-096 Aphena Pharma Solutions - Tennessee, LLC 30 TABLET in 1 BOTTLE, PLASTIC (71610-096-30) July 13, 2018
71610-096-45 71610-096 Aphena Pharma Solutions - Tennessee, LLC 45 TABLET in 1 BOTTLE, PLASTIC (71610-096-45) May 31, 2024
71610-096-53 71610-096 Aphena Pharma Solutions - Tennessee, LLC 60 TABLET in 1 BOTTLE, PLASTIC (71610-096-53) July 13, 2018
71610-096-60 71610-096 Aphena Pharma Solutions - Tennessee, LLC 90 TABLET in 1 BOTTLE, PLASTIC (71610-096-60) July 13, 2018
71610-096-80 71610-096 Aphena Pharma Solutions - Tennessee, LLC 180 TABLET in 1 BOTTLE, PLASTIC (71610-096-80) July 13, 2018
71610-634-30 71610-634 Aphena Pharma Solutions - Tennessee, LLC 30 TABLET in 1 BOTTLE (71610-634-30) February 22, 2022
71610-634-45 71610-634 Aphena Pharma Solutions - Tennessee, LLC 45 TABLET in 1 BOTTLE (71610-634-45) February 22, 2022
71610-634-53 71610-634 Aphena Pharma Solutions - Tennessee, LLC 60 TABLET in 1 BOTTLE (71610-634-53) February 22, 2022
71610-634-60 71610-634 Aphena Pharma Solutions - Tennessee, LLC 90 TABLET in 1 BOTTLE (71610-634-60) February 22, 2022
71610-634-80 71610-634 Aphena Pharma Solutions - Tennessee, LLC 180 TABLET in 1 BOTTLE (71610-634-80) February 22, 2022
71610-635-30 71610-635 Aphena Pharma Solutions - Tennessee, LLC 30 TABLET in 1 BOTTLE (71610-635-30) February 22, 2022
71610-635-45 71610-635 Aphena Pharma Solutions - Tennessee, LLC 45 TABLET in 1 BOTTLE (71610-635-45) March 8, 2022
71610-635-53 71610-635 Aphena Pharma Solutions - Tennessee, LLC 60 TABLET in 1 BOTTLE (71610-635-53) February 22, 2022
71610-635-60 71610-635 Aphena Pharma Solutions - Tennessee, LLC 90 TABLET in 1 BOTTLE (71610-635-60) February 22, 2022
71610-635-80 71610-635 Aphena Pharma Solutions - Tennessee, LLC 180 TABLET in 1 BOTTLE (71610-635-80) February 22, 2022
71610-635-92 71610-635 Aphena Pharma Solutions - Tennessee, LLC 270 TABLET in 1 BOTTLE (71610-635-92) February 22, 2022
71610-636-30 71610-636 Aphena Pharma Solutions - Tennessee, LLC 30 TABLET in 1 BOTTLE (71610-636-30) February 24, 2022
71610-636-45 71610-636 Aphena Pharma Solutions - Tennessee, LLC 45 TABLET in 1 BOTTLE (71610-636-45) February 24, 2022
71610-636-53 71610-636 Aphena Pharma Solutions - Tennessee, LLC 60 TABLET in 1 BOTTLE (71610-636-53) February 24, 2022
71610-636-60 71610-636 Aphena Pharma Solutions - Tennessee, LLC 90 TABLET in 1 BOTTLE (71610-636-60) February 24, 2022
71610-636-80 71610-636 Aphena Pharma Solutions - Tennessee, LLC 180 TABLET in 1 BOTTLE (71610-636-80) February 24, 2022
71610-843-30 71610-843 Aphena Pharma Solutions - Tennessee, LLC 30 TABLET in 1 BOTTLE (71610-843-30) June 26, 2024
71610-843-53 71610-843 Aphena Pharma Solutions - Tennessee, LLC 60 TABLET in 1 BOTTLE (71610-843-53) June 26, 2024
71610-843-60 71610-843 Aphena Pharma Solutions - Tennessee, LLC 90 TABLET in 1 BOTTLE (71610-843-60) June 26, 2024
71610-843-80 71610-843 Aphena Pharma Solutions - Tennessee, LLC 180 TABLET in 1 BOTTLE (71610-843-80) June 26, 2024
71610-951-30 71610-951 Aphena Pharma Solutions - Tennessee, LLC 30 TABLET in 1 BOTTLE (71610-951-30) October 13, 2025
71610-951-45 71610-951 Aphena Pharma Solutions - Tennessee, LLC 45 TABLET in 1 BOTTLE (71610-951-45) September 19, 2025
71610-951-53 71610-951 Aphena Pharma Solutions - Tennessee, LLC 60 TABLET in 1 BOTTLE (71610-951-53) September 19, 2025
71610-951-60 71610-951 Aphena Pharma Solutions - Tennessee, LLC 90 TABLET in 1 BOTTLE (71610-951-60) September 19, 2025
71610-951-80 71610-951 Aphena Pharma Solutions - Tennessee, LLC 180 TABLET in 1 BOTTLE (71610-951-80) September 19, 2025
59651-796-01 59651-796 Aurobindo Pharma Limited 100 TABLET in 1 BOTTLE (59651-796-01) July 17, 2025
59651-796-91 59651-796 Aurobindo Pharma Limited 100000 TABLET in 1 BAG (59651-796-91) July 17, 2025
59651-796-99 59651-796 Aurobindo Pharma Limited 1000 TABLET in 1 BOTTLE (59651-796-99) July 17, 2025
59651-797-01 59651-797 Aurobindo Pharma Limited 100 TABLET in 1 BOTTLE (59651-797-01) July 17, 2025
59651-797-72 59651-797 Aurobindo Pharma Limited 75000 TABLET in 1 BAG (59651-797-72) July 17, 2025
59651-797-99 59651-797 Aurobindo Pharma Limited 1000 TABLET in 1 BOTTLE (59651-797-99) July 17, 2025
59651-798-01 59651-798 Aurobindo Pharma Limited 100 TABLET in 1 BOTTLE (59651-798-01) July 17, 2025
59651-798-05 59651-798 Aurobindo Pharma Limited 500 TABLET in 1 BOTTLE (59651-798-05) July 17, 2025
59651-798-62 59651-798 Aurobindo Pharma Limited 30000 TABLET in 1 BAG (59651-798-62) July 17, 2025
42291-468-01 42291-468 AvKARE 100 TABLET in 1 BOTTLE (42291-468-01) January 4, 2022
42291-468-10 42291-468 AvKARE 1000 TABLET in 1 BOTTLE (42291-468-10) January 4, 2022
42291-468-90 42291-468 AvKARE 90 TABLET in 1 BOTTLE (42291-468-90) January 4, 2022
42291-469-01 42291-469 AvKARE 100 TABLET in 1 BOTTLE (42291-469-01) January 4, 2022
42291-469-10 42291-469 AvKARE 1000 TABLET in 1 BOTTLE (42291-469-10) January 4, 2022
42291-469-90 42291-469 AvKARE 90 TABLET in 1 BOTTLE (42291-469-90) January 4, 2022
42291-470-01 42291-470 AvKARE 100 TABLET in 1 BOTTLE (42291-470-01) January 4, 2022
42291-470-50 42291-470 AvKARE 500 TABLET in 1 BOTTLE (42291-470-50) January 4, 2022
63629-1119-1 63629-1119 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE, PLASTIC (63629-1119-1) July 30, 2020
63629-1120-1 63629-1120 Bryant Ranch Prepack 500 TABLET in 1 BOTTLE, PLASTIC (63629-1120-1) July 30, 2020
63629-1214-1 63629-1214 Bryant Ranch Prepack 1000 TABLET in 1 BOTTLE (63629-1214-1) January 14, 2021
63629-1215-1 63629-1215 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE (63629-1215-1) January 14, 2021
63629-1216-1 63629-1216 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE (63629-1216-1) January 14, 2021
63629-1217-1 63629-1217 Bryant Ranch Prepack 1000 TABLET in 1 BOTTLE (63629-1217-1) January 14, 2021
71335-0384-1 71335-0384 Bryant Ranch Prepack 30 TABLET in 1 BOTTLE (71335-0384-1) February 9, 2022
71335-0384-2 71335-0384 Bryant Ranch Prepack 90 TABLET in 1 BOTTLE (71335-0384-2) February 9, 2022
71335-0384-3 71335-0384 Bryant Ranch Prepack 60 TABLET in 1 BOTTLE (71335-0384-3) February 9, 2022
71335-0384-4 71335-0384 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE (71335-0384-4) February 9, 2022
71335-0384-5 71335-0384 Bryant Ranch Prepack 7 TABLET in 1 BOTTLE (71335-0384-5) February 9, 2022
71335-0384-6 71335-0384 Bryant Ranch Prepack 28 TABLET in 1 BOTTLE (71335-0384-6) February 9, 2022
71335-0384-7 71335-0384 Bryant Ranch Prepack 14 TABLET in 1 BOTTLE (71335-0384-7) February 9, 2022
71335-0384-8 71335-0384 Bryant Ranch Prepack 10 TABLET in 1 BOTTLE (71335-0384-8) February 9, 2022
71335-0384-9 71335-0384 Bryant Ranch Prepack 20 TABLET in 1 BOTTLE (71335-0384-9) February 9, 2022
71335-0842-1 71335-0842 Bryant Ranch Prepack 40 TABLET in 1 BOTTLE (71335-0842-1) May 31, 2018
71335-0842-2 71335-0842 Bryant Ranch Prepack 30 TABLET in 1 BOTTLE (71335-0842-2) May 31, 2018
71335-0842-3 71335-0842 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE (71335-0842-3) May 31, 2018
71335-0842-4 71335-0842 Bryant Ranch Prepack 90 TABLET in 1 BOTTLE (71335-0842-4) May 31, 2018
71335-0842-5 71335-0842 Bryant Ranch Prepack 60 TABLET in 1 BOTTLE (71335-0842-5) May 31, 2018
71335-0842-6 71335-0842 Bryant Ranch Prepack 7 TABLET in 1 BOTTLE (71335-0842-6) May 31, 2018
71335-0842-7 71335-0842 Bryant Ranch Prepack 14 TABLET in 1 BOTTLE (71335-0842-7) May 31, 2018
71335-0842-8 71335-0842 Bryant Ranch Prepack 180 TABLET in 1 BOTTLE (71335-0842-8) May 31, 2018
71335-0842-9 71335-0842 Bryant Ranch Prepack 10 TABLET in 1 BOTTLE (71335-0842-9) May 31, 2018
71335-0852-1 71335-0852 Bryant Ranch Prepack 30 TABLET in 1 BOTTLE (71335-0852-1) June 22, 2018
71335-0852-2 71335-0852 Bryant Ranch Prepack 90 TABLET in 1 BOTTLE (71335-0852-2) June 22, 2018
71335-0852-3 71335-0852 Bryant Ranch Prepack 60 TABLET in 1 BOTTLE (71335-0852-3) June 22, 2018
71335-0852-4 71335-0852 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE (71335-0852-4) June 22, 2018
71335-0852-5 71335-0852 Bryant Ranch Prepack 7 TABLET in 1 BOTTLE (71335-0852-5) June 22, 2018
71335-0852-6 71335-0852 Bryant Ranch Prepack 28 TABLET in 1 BOTTLE (71335-0852-6) June 22, 2018
71335-0852-7 71335-0852 Bryant Ranch Prepack 14 TABLET in 1 BOTTLE (71335-0852-7) June 22, 2018
71335-0852-8 71335-0852 Bryant Ranch Prepack 10 TABLET in 1 BOTTLE (71335-0852-8) June 22, 2018
71335-0852-9 71335-0852 Bryant Ranch Prepack 20 TABLET in 1 BOTTLE (71335-0852-9) June 22, 2018
71335-2317-1 71335-2317 Bryant Ranch Prepack 40 TABLET in 1 BOTTLE (71335-2317-1) January 2, 2024
71335-2317-2 71335-2317 Bryant Ranch Prepack 30 TABLET in 1 BOTTLE (71335-2317-2) January 2, 2024
71335-2317-3 71335-2317 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE (71335-2317-3) January 2, 2024
71335-2317-4 71335-2317 Bryant Ranch Prepack 90 TABLET in 1 BOTTLE (71335-2317-4) January 2, 2024
71335-2317-5 71335-2317 Bryant Ranch Prepack 60 TABLET in 1 BOTTLE (71335-2317-5) January 2, 2024
71335-2317-6 71335-2317 Bryant Ranch Prepack 7 TABLET in 1 BOTTLE (71335-2317-6) January 2, 2024
71335-2317-7 71335-2317 Bryant Ranch Prepack 14 TABLET in 1 BOTTLE (71335-2317-7) January 2, 2024
71335-2317-8 71335-2317 Bryant Ranch Prepack 180 TABLET in 1 BOTTLE (71335-2317-8) January 2, 2024
71335-2317-9 71335-2317 Bryant Ranch Prepack 10 TABLET in 1 BOTTLE (71335-2317-9) January 2, 2024
71335-2319-0 71335-2319 Bryant Ranch Prepack 6 TABLET in 1 BOTTLE (71335-2319-0) January 4, 2024
71335-2319-1 71335-2319 Bryant Ranch Prepack 30 TABLET in 1 BOTTLE (71335-2319-1) January 4, 2024
71335-2319-2 71335-2319 Bryant Ranch Prepack 90 TABLET in 1 BOTTLE (71335-2319-2) January 4, 2024
71335-2319-3 71335-2319 Bryant Ranch Prepack 60 TABLET in 1 BOTTLE (71335-2319-3) January 4, 2024
71335-2319-4 71335-2319 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE (71335-2319-4) January 4, 2024
71335-2319-5 71335-2319 Bryant Ranch Prepack 7 TABLET in 1 BOTTLE (71335-2319-5) January 4, 2024
71335-2319-6 71335-2319 Bryant Ranch Prepack 28 TABLET in 1 BOTTLE (71335-2319-6) January 4, 2024
71335-2319-7 71335-2319 Bryant Ranch Prepack 14 TABLET in 1 BOTTLE (71335-2319-7) January 4, 2024
71335-2319-8 71335-2319 Bryant Ranch Prepack 10 TABLET in 1 BOTTLE (71335-2319-8) January 4, 2024
71335-2319-9 71335-2319 Bryant Ranch Prepack 20 TABLET in 1 BOTTLE (71335-2319-9) January 4, 2024
72162-1360-0 72162-1360 Bryant Ranch Prepack 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1360-0) February 2, 2024
72162-1360-1 72162-1360 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE, PLASTIC (72162-1360-1) February 2, 2024
72162-1361-0 72162-1361 Bryant Ranch Prepack 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1361-0) October 4, 2023
72162-1361-1 72162-1361 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE, PLASTIC (72162-1361-1) October 4, 2023
72162-1362-1 72162-1362 Bryant Ranch Prepack 100 TABLET in 1 BOTTLE, PLASTIC (72162-1362-1) February 2, 2024
72162-1362-5 72162-1362 Bryant Ranch Prepack 500 TABLET in 1 BOTTLE, PLASTIC (72162-1362-5) February 2, 2024
17224-178-21 17224-178 Calvin Scott & Co., Inc. 21 TABLET in 1 BOTTLE (17224-178-21) May 15, 2016
17224-178-30 17224-178 Calvin Scott & Co., Inc. 30 TABLET in 1 BOTTLE (17224-178-30) May 15, 2016
17224-185-21 17224-185 Calvin Scott & Co., Inc. 21 TABLET in 1 BOTTLE, PLASTIC (17224-185-21) May 15, 2016
55154-2348-0 55154-2348 Cardinal Health 107, LLC 10 BLISTER PACK in 1 BAG (55154-2348-0) / 1 TABLET in 1 BLISTER PACK December 4, 2024
55154-2349-0 55154-2349 Cardinal Health 107, LLC 10 BLISTER PACK in 1 BAG (55154-2349-0) / 1 TABLET in 1 BLISTER PACK December 4, 2024
62135-753-90 62135-753 Chartwell RX, LLC 90 TABLET in 1 PACKAGE (62135-753-90) April 17, 2024
62135-754-90 62135-754 Chartwell RX, LLC 90 TABLET in 1 PACKAGE (62135-754-90) April 17, 2024
67046-0768-3 67046-0768 Coupler LLC 30 TABLET in 1 BLISTER PACK (67046-0768-3) June 10, 2026
67046-1555-3 67046-1555 Coupler LLC 30 TABLET in 1 BLISTER PACK (67046-1555-3) April 29, 2025
67046-1589-3 67046-1589 Coupler LLC 30 TABLET in 1 BLISTER PACK (67046-1589-3) September 16, 2025
67046-1663-3 67046-1663 Coupler LLC 30 TABLET in 1 BLISTER PACK (67046-1663-3) March 11, 2026
61919-242-30 61919-242 DIRECT RX 30 TABLET in 1 BOTTLE (61919-242-30) June 18, 2020
61919-242-90 61919-242 DIRECT RX 90 TABLET in 1 BOTTLE (61919-242-90) June 18, 2020
61919-255-30 61919-255 Direct_Rx 30 TABLET in 1 BOTTLE (61919-255-30) October 21, 2021
61919-255-90 61919-255 Direct_Rx 90 TABLET in 1 BOTTLE (61919-255-90) October 21, 2021
63561-0164-1 63561-0164 Granulation Technology, Inc. 100 TABLET in 1 BOTTLE (63561-0164-1) January 15, 2026
63561-0164-2 63561-0164 Granulation Technology, Inc. 1000 TABLET in 1 BOTTLE (63561-0164-2) December 18, 2025
63561-0164-9 63561-0164 Granulation Technology, Inc. 90 TABLET in 1 BOTTLE (63561-0164-9) December 18, 2025
63561-0165-1 63561-0165 Granulation Technology, Inc. 100 TABLET in 1 BOTTLE (63561-0165-1) January 15, 2026
63561-0165-2 63561-0165 Granulation Technology, Inc. 1000 TABLET in 1 BOTTLE (63561-0165-2) December 18, 2025
63561-0165-9 63561-0165 Granulation Technology, Inc. 90 TABLET in 1 BOTTLE (63561-0165-9) December 18, 2025
63561-0166-1 63561-0166 Granulation Technology, Inc. 100 TABLET in 1 BOTTLE (63561-0166-1) January 15, 2026
63561-0166-5 63561-0166 Granulation Technology, Inc. 500 TABLET in 1 BOTTLE (63561-0166-5) December 18, 2025
63561-0166-9 63561-0166 Granulation Technology, Inc. 90 TABLET in 1 BOTTLE (63561-0166-9) December 18, 2025
0054-4297-25 0054-4297 Hikma Pharmaceuticals USA Inc. 100 TABLET in 1 BOTTLE, PLASTIC (0054-4297-25) November 10, 1983
0054-4297-31 0054-4297 Hikma Pharmaceuticals USA Inc. 1000 TABLET in 1 BOTTLE, PLASTIC (0054-4297-31) November 10, 1983
0054-4299-25 0054-4299 Hikma Pharmaceuticals USA Inc. 100 TABLET in 1 BOTTLE (0054-4299-25) November 10, 1983
0054-4299-31 0054-4299 Hikma Pharmaceuticals USA Inc. 1000 TABLET in 1 BOTTLE (0054-4299-31) November 10, 1983
0054-4301-25 0054-4301 Hikma Pharmaceuticals USA Inc. 100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25) March 13, 1991
0054-4301-29 0054-4301 Hikma Pharmaceuticals USA Inc. 500 TABLET in 1 BOTTLE, PLASTIC (0054-4301-29) March 13, 1991
0054-8297-25 0054-8297 Hikma Pharmaceuticals USA Inc. 10 BLISTER PACK in 1 CARTON (0054-8297-25) / 10 TABLET in 1 BLISTER PACK November 10, 1983
0054-8299-25 0054-8299 Hikma Pharmaceuticals USA Inc. 10 BLISTER PACK in 1 CARTON (0054-8299-25) / 10 TABLET in 1 BLISTER PACK November 10, 1983
0054-8301-25 0054-8301 Hikma Pharmaceuticals USA Inc. 10 BLISTER PACK in 1 CARTON (0054-8301-25) / 10 TABLET in 1 BLISTER PACK March 13, 1991
83980-002-01 83980-002 Ipca Laboratories Limited 100 TABLET in 1 BOTTLE (83980-002-01) June 3, 2024
83980-002-10 83980-002 Ipca Laboratories Limited 1000 TABLET in 1 BOTTLE (83980-002-10) June 3, 2024
83980-002-97 83980-002 Ipca Laboratories Limited 10 TABLET in 1 BOTTLE (83980-002-97) June 3, 2024
83980-003-01 83980-003 Ipca Laboratories Limited 100 TABLET in 1 BOTTLE (83980-003-01) June 3, 2024
83980-003-10 83980-003 Ipca Laboratories Limited 1000 TABLET in 1 BOTTLE (83980-003-10) June 3, 2024
83980-003-97 83980-003 Ipca Laboratories Limited 10 TABLET in 1 BOTTLE (83980-003-97) June 3, 2024
83980-004-01 83980-004 Ipca Laboratories Limited 100 TABLET in 1 BOTTLE (83980-004-01) June 3, 2024
83980-004-05 83980-004 Ipca Laboratories Limited 500 TABLET in 1 BOTTLE (83980-004-05) June 3, 2024
83980-004-10 83980-004 Ipca Laboratories Limited 1000 TABLET in 1 BOTTLE (83980-004-10) June 3, 2024
83980-004-97 83980-004 Ipca Laboratories Limited 10 TABLET in 1 BOTTLE (83980-004-97) June 3, 2024
69315-116-01 69315-116 Leading Pharma, LLC 100 TABLET in 1 BOTTLE (69315-116-01) May 15, 2016
69315-116-10 69315-116 Leading Pharma, LLC 1000 TABLET in 1 BOTTLE (69315-116-10) May 15, 2016
69315-117-01 69315-117 Leading Pharma, LLC 100 TABLET in 1 BOTTLE (69315-117-01) May 15, 2016
69315-117-10 69315-117 Leading Pharma, LLC 1000 TABLET in 1 BOTTLE (69315-117-10) May 15, 2016
69315-118-01 69315-118 Leading Pharma, LLC 100 TABLET in 1 BOTTLE (69315-118-01) May 15, 2016
69315-118-05 69315-118 Leading Pharma, LLC 500 TABLET in 1 BOTTLE (69315-118-05) May 15, 2016
0904-7177-61 0904-7177 Major Pharmaceuticals 100 BLISTER PACK in 1 CARTON (0904-7177-61) / 1 TABLET in 1 BLISTER PACK March 26, 2004
0904-7178-61 0904-7178 Major Pharmaceuticals 100 BLISTER PACK in 1 CARTON (0904-7178-61) / 1 TABLET in 1 BLISTER PACK March 26, 2004
10135-832-01 10135-832 Marlex Pharmaceuticals, Inc. 100 TABLET in 1 BOTTLE (10135-832-01) March 1, 2026
10135-832-10 10135-832 Marlex Pharmaceuticals, Inc. 1000 TABLET in 1 BOTTLE (10135-832-10) March 1, 2026
10135-832-90 10135-832 Marlex Pharmaceuticals, Inc. 90 TABLET in 1 BOTTLE (10135-832-90) March 1, 2026
10135-833-01 10135-833 Marlex Pharmaceuticals, Inc. 100 TABLET in 1 BOTTLE (10135-833-01) March 1, 2026
10135-833-10 10135-833 Marlex Pharmaceuticals, Inc. 1000 TABLET in 1 BOTTLE (10135-833-10) March 1, 2026
10135-833-90 10135-833 Marlex Pharmaceuticals, Inc. 90 TABLET in 1 BOTTLE (10135-833-90) March 1, 2026
10135-834-01 10135-834 Marlex Pharmaceuticals, Inc. 100 TABLET in 1 BOTTLE (10135-834-01) March 1, 2026
10135-834-05 10135-834 Marlex Pharmaceuticals, Inc. 500 TABLET in 1 BOTTLE (10135-834-05) March 1, 2026
10135-834-90 10135-834 Marlex Pharmaceuticals, Inc. 90 TABLET in 1 BOTTLE (10135-834-90) March 1, 2026
0615-8368-05 0615-8368 NCS HealthCare of KY, LLC dba Vangard Labs 15 TABLET in 1 BLISTER PACK (0615-8368-05) December 8, 2020
0615-8368-07 0615-8368 NCS HealthCare of KY, LLC dba Vangard Labs 7 TABLET in 1 BLISTER PACK (0615-8368-07) June 21, 2022
0615-8368-10 0615-8368 NCS HealthCare of KY, LLC dba Vangard Labs 10 TABLET in 1 BLISTER PACK (0615-8368-10) November 18, 2022
0615-8368-14 0615-8368 NCS HealthCare of KY, LLC dba Vangard Labs 14 TABLET in 1 BLISTER PACK (0615-8368-14) June 21, 2022
0615-8368-28 0615-8368 NCS HealthCare of KY, LLC dba Vangard Labs 28 TABLET in 1 BLISTER PACK (0615-8368-28) April 15, 2024
0615-8368-30 0615-8368 NCS HealthCare of KY, LLC dba Vangard Labs 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8368-30) / 5 TABLET in 1 BLISTER PACK December 14, 2020
0615-8368-39 0615-8368 NCS HealthCare of KY, LLC dba Vangard Labs 30 TABLET in 1 BLISTER PACK (0615-8368-39) December 8, 2020
0615-8369-05 0615-8369 NCS HealthCare of KY, LLC dba Vangard Labs 15 TABLET in 1 BLISTER PACK (0615-8369-05) December 4, 2020
0615-8369-07 0615-8369 NCS HealthCare of KY, LLC dba Vangard Labs 7 TABLET in 1 BLISTER PACK (0615-8369-07) June 2, 2022
0615-8369-14 0615-8369 NCS HealthCare of KY, LLC dba Vangard Labs 14 TABLET in 1 BLISTER PACK (0615-8369-14) June 2, 2022
0615-8369-30 0615-8369 NCS HealthCare of KY, LLC dba Vangard Labs 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8369-30) / 5 TABLET in 1 BLISTER PACK December 16, 2020
0615-8369-39 0615-8369 NCS HealthCare of KY, LLC dba Vangard Labs 30 TABLET in 1 BLISTER PACK (0615-8369-39) December 4, 2020
0615-8370-39 0615-8370 NCS HealthCare of KY, LLC dba Vangard Labs 30 TABLET in 1 BLISTER PACK (0615-8370-39) December 15, 2020
51655-269-25 51655-269 Northwind Health Company, LLC 60 TABLET in 1 BOTTLE, PLASTIC (51655-269-25) February 9, 2023
51655-269-26 51655-269 Northwind Health Company, LLC 90 TABLET in 1 BOTTLE, PLASTIC (51655-269-26) September 6, 2022
51655-269-52 51655-269 Northwind Health Company, LLC 30 TABLET in 1 BOTTLE, PLASTIC (51655-269-52) August 8, 2022
51655-269-53 51655-269 Northwind Health Company, LLC 10 TABLET in 1 BOTTLE, PLASTIC (51655-269-53) February 9, 2023
51655-310-53 51655-310 Northwind Health Company, LLC 10 TABLET in 1 BOTTLE, PLASTIC (51655-310-53) November 28, 2022
51655-481-52 51655-481 Northwind Health Company, LLC 30 TABLET in 1 BOTTLE, PLASTIC (51655-481-52) November 19, 2020
51655-481-53 51655-481 Northwind Health Company, LLC 10 TABLET in 1 BOTTLE, PLASTIC (51655-481-53) November 30, 2020
51655-517-26 51655-517 Northwind Health Company, LLC 90 TABLET in 1 BOTTLE, PLASTIC (51655-517-26) July 11, 2022
51655-517-52 51655-517 Northwind Health Company, LLC 30 TABLET in 1 BOTTLE, PLASTIC (51655-517-52) June 24, 2022
82868-050-30 82868-050 Northwind Health Company, LLC 30 TABLET in 1 BOTTLE, PLASTIC (82868-050-30) February 29, 2024
82868-050-90 82868-050 Northwind Health Company, LLC 90 TABLET in 1 BOTTLE, PLASTIC (82868-050-90) February 29, 2024
68071-3673-3 68071-3673 NuCare Pharmaceuticals, Inc. 30 TABLET in 1 BOTTLE (68071-3673-3) August 30, 2024
68071-3673-9 68071-3673 NuCare Pharmaceuticals, Inc. 90 TABLET in 1 BOTTLE (68071-3673-9) October 16, 2025
68071-1708-1 68071-1708 NuCare Pharmaceuticals,Inc. 100 TABLET in 1 BOTTLE (68071-1708-1) February 6, 2019
68071-1809-1 68071-1809 NuCare Pharmaceuticals,Inc. 100 TABLET in 1 BOTTLE (68071-1809-1) January 29, 2019
68071-2360-1 68071-2360 NuCare Pharmaceuticals,Inc. 100 TABLET in 1 BOTTLE, PLASTIC (68071-2360-1) March 11, 2021
68071-3273-3 68071-3273 NuCare Pharmaceuticals,Inc. 30 TABLET in 1 BOTTLE (68071-3273-3) January 29, 2019
68071-3273-6 68071-3273 NuCare Pharmaceuticals,Inc. 60 TABLET in 1 BOTTLE (68071-3273-6) December 19, 2023
68071-3273-9 68071-3273 NuCare Pharmaceuticals,Inc. 90 TABLET in 1 BOTTLE (68071-3273-9) December 19, 2023
68071-3536-3 68071-3536 NuCare Pharmaceuticals,Inc. 30 TABLET in 1 BOTTLE (68071-3536-3) November 28, 2023
68071-3536-9 68071-3536 NuCare Pharmaceuticals,Inc. 90 TABLET in 1 BOTTLE (68071-3536-9) September 14, 2026
68071-4445-1 68071-4445 NuCare Pharmaceuticals,Inc. 10 TABLET in 1 BOTTLE (68071-4445-1) May 21, 2018
68071-4445-2 68071-4445 NuCare Pharmaceuticals,Inc. 20 TABLET in 1 BOTTLE (68071-4445-2) May 21, 2018
68071-4445-3 68071-4445 NuCare Pharmaceuticals,Inc. 30 TABLET in 1 BOTTLE (68071-4445-3) May 21, 2018
68071-4445-4 68071-4445 NuCare Pharmaceuticals,Inc. 40 TABLET in 1 BOTTLE (68071-4445-4) May 21, 2018
68071-4445-6 68071-4445 NuCare Pharmaceuticals,Inc. 60 TABLET in 1 BOTTLE (68071-4445-6) May 21, 2018
68071-4445-8 68071-4445 NuCare Pharmaceuticals,Inc. 180 TABLET in 1 BOTTLE (68071-4445-8) May 21, 2018
68071-4445-9 68071-4445 NuCare Pharmaceuticals,Inc. 90 TABLET in 1 BOTTLE (68071-4445-9) May 21, 2018
68071-4522-1 68071-4522 NuCare Pharmaceuticals,Inc. 100 TABLET in 1 BOTTLE (68071-4522-1) August 10, 2018
68071-4534-1 68071-4534 NuCare Pharmaceuticals,Inc. 100 TABLET in 1 BOTTLE (68071-4534-1) August 20, 2018
43063-702-21 43063-702 PD-Rx Pharmaceuticals, Inc. 21 TABLET in 1 BOTTLE, PLASTIC (43063-702-21) January 31, 2017
43063-702-30 43063-702 PD-Rx Pharmaceuticals, Inc. 30 TABLET in 1 BOTTLE, PLASTIC (43063-702-30) September 29, 2016
43063-702-60 43063-702 PD-Rx Pharmaceuticals, Inc. 60 TABLET in 1 BOTTLE, PLASTIC (43063-702-60) August 10, 2016
43063-702-79 43063-702 PD-Rx Pharmaceuticals, Inc. 1 TABLET in 1 BOTTLE, PLASTIC (43063-702-79) February 21, 2017
43063-702-90 43063-702 PD-Rx Pharmaceuticals, Inc. 90 TABLET in 1 BOTTLE, PLASTIC (43063-702-90) January 4, 2017
43063-716-01 43063-716 PD-Rx Pharmaceuticals, Inc. 100 TABLET in 1 BOTTLE, PLASTIC (43063-716-01) May 16, 2017
43063-716-30 43063-716 PD-Rx Pharmaceuticals, Inc. 30 TABLET in 1 BOTTLE, PLASTIC (43063-716-30) October 12, 2016
43063-716-60 43063-716 PD-Rx Pharmaceuticals, Inc. 60 TABLET in 1 BOTTLE, PLASTIC (43063-716-60) October 16, 2016
43063-716-90 43063-716 PD-Rx Pharmaceuticals, Inc. 90 TABLET in 1 BOTTLE, PLASTIC (43063-716-90) January 6, 2017
43063-849-21 43063-849 PD-Rx Pharmaceuticals, Inc. 21 TABLET in 1 BOTTLE, PLASTIC (43063-849-21) April 27, 2018
43063-849-30 43063-849 PD-Rx Pharmaceuticals, Inc. 30 TABLET in 1 BOTTLE, PLASTIC (43063-849-30) April 27, 2018
43063-849-60 43063-849 PD-Rx Pharmaceuticals, Inc. 60 TABLET in 1 BOTTLE, PLASTIC (43063-849-60) May 3, 2018
43063-849-90 43063-849 PD-Rx Pharmaceuticals, Inc. 90 TABLET in 1 BOTTLE, PLASTIC (43063-849-90) May 3, 2018
72789-030-30 72789-030 PD-Rx Pharmaceuticals, Inc. 30 TABLET in 1 BOTTLE, PLASTIC (72789-030-30) December 5, 2019
72789-030-60 72789-030 PD-Rx Pharmaceuticals, Inc. 60 TABLET in 1 BOTTLE, PLASTIC (72789-030-60) December 5, 2019
72789-032-30 72789-032 PD-Rx Pharmaceuticals, Inc. 30 TABLET in 1 BOTTLE, PLASTIC (72789-032-30) December 9, 2019
72789-032-60 72789-032 PD-Rx Pharmaceuticals, Inc. 60 TABLET in 1 BOTTLE, PLASTIC (72789-032-60) December 9, 2019
72789-033-01 72789-033 PD-Rx Pharmaceuticals, Inc. 100 TABLET in 1 BOTTLE, PLASTIC (72789-033-01) March 9, 2021
72789-033-30 72789-033 PD-Rx Pharmaceuticals, Inc. 30 TABLET in 1 BOTTLE, PLASTIC (72789-033-30) December 9, 2019
72789-033-60 72789-033 PD-Rx Pharmaceuticals, Inc. 60 TABLET in 1 BOTTLE, PLASTIC (72789-033-60) December 9, 2019
72789-033-82 72789-033 PD-Rx Pharmaceuticals, Inc. 500 TABLET in 1 BOTTLE, PLASTIC (72789-033-82) March 9, 2021
72789-157-01 72789-157 PD-Rx Pharmaceuticals, Inc. 100 TABLET in 1 BOTTLE, PLASTIC (72789-157-01) January 12, 2021
68788-6948-1 68788-6948 Preferred Pharmaceuticals Inc. 100 TABLET in 1 BOTTLE (68788-6948-1) April 17, 2017
68788-6948-3 68788-6948 Preferred Pharmaceuticals Inc. 30 TABLET in 1 BOTTLE (68788-6948-3) April 17, 2017
68788-6948-6 68788-6948 Preferred Pharmaceuticals Inc. 60 TABLET in 1 BOTTLE (68788-6948-6) April 17, 2017
68788-6948-9 68788-6948 Preferred Pharmaceuticals Inc. 90 TABLET in 1 BOTTLE (68788-6948-9) April 17, 2017
68788-8799-1 68788-8799 Preferred Pharmaceuticals Inc. 100 TABLET in 1 BOTTLE (68788-8799-1) January 1, 2025
68788-8799-3 68788-8799 Preferred Pharmaceuticals Inc. 30 TABLET in 1 BOTTLE (68788-8799-3) January 1, 2025
68788-8799-6 68788-8799 Preferred Pharmaceuticals Inc. 60 TABLET in 1 BOTTLE (68788-8799-6) January 1, 2025
68788-8799-9 68788-8799 Preferred Pharmaceuticals Inc. 90 TABLET in 1 BOTTLE (68788-8799-9) January 1, 2025
68788-6784-1 68788-6784 Preferred Pharmaceuticals, Inc. 100 TABLET in 1 BOTTLE (68788-6784-1) October 25, 2016
68788-6784-3 68788-6784 Preferred Pharmaceuticals, Inc. 30 TABLET in 1 BOTTLE (68788-6784-3) October 25, 2016
68788-6784-6 68788-6784 Preferred Pharmaceuticals, Inc. 60 TABLET in 1 BOTTLE (68788-6784-6) October 25, 2016
68788-6784-9 68788-6784 Preferred Pharmaceuticals, Inc. 90 TABLET in 1 BOTTLE (68788-6784-9) October 25, 2016
68788-8870-1 68788-8870 Prefferred Pharmaceuticals Inc. 100 TABLET in 1 BOTTLE (68788-8870-1) April 30, 2025
68788-8870-3 68788-8870 Prefferred Pharmaceuticals Inc. 30 TABLET in 1 BOTTLE (68788-8870-3) April 30, 2025
68788-8870-6 68788-8870 Prefferred Pharmaceuticals Inc. 60 TABLET in 1 BOTTLE (68788-8870-6) April 30, 2025
68788-8870-9 68788-8870 Prefferred Pharmaceuticals Inc. 90 TABLET in 1 BOTTLE (68788-8870-9) April 30, 2025
63187-506-30 63187-506 Proficient Rx LP 30 TABLET in 1 BOTTLE (63187-506-30) December 1, 2018
63187-506-60 63187-506 Proficient Rx LP 60 TABLET in 1 BOTTLE (63187-506-60) December 1, 2018
63187-506-90 63187-506 Proficient Rx LP 90 TABLET in 1 BOTTLE (63187-506-90) December 1, 2018
63187-517-30 63187-517 Proficient Rx LP 30 TABLET in 1 BOTTLE (63187-517-30) December 1, 2018
63187-517-60 63187-517 Proficient Rx LP 60 TABLET in 1 BOTTLE (63187-517-60) December 1, 2018
63187-517-90 63187-517 Proficient Rx LP 90 TABLET in 1 BOTTLE (63187-517-90) December 1, 2018
63187-739-10 63187-739 Proficient Rx LP 10 TABLET in 1 BOTTLE (63187-739-10) March 1, 2017
63187-739-30 63187-739 Proficient Rx LP 30 TABLET in 1 BOTTLE (63187-739-30) October 3, 2016
63187-739-60 63187-739 Proficient Rx LP 60 TABLET in 1 BOTTLE (63187-739-60) October 3, 2016
63187-739-90 63187-739 Proficient Rx LP 90 TABLET in 1 BOTTLE (63187-739-90) October 3, 2016
63187-790-07 63187-790 Proficient Rx LP 7 TABLET in 1 BOTTLE (63187-790-07) July 18, 2025
63187-790-30 63187-790 Proficient Rx LP 30 TABLET in 1 BOTTLE (63187-790-30) December 1, 2016
63187-790-60 63187-790 Proficient Rx LP 60 TABLET in 1 BOTTLE (63187-790-60) December 1, 2016
63187-790-90 63187-790 Proficient Rx LP 90 TABLET in 1 BOTTLE (63187-790-90) December 1, 2016
42708-123-30 42708-123 QPharma Inc 30 TABLET in 1 BOTTLE (42708-123-30) May 23, 2018
70518-0050-0 70518-0050 REMEDYREPACK INC. 30 TABLET in 1 BLISTER PACK (70518-0050-0) December 12, 2016
70518-0050-1 70518-0050 REMEDYREPACK INC. 90 TABLET in 1 BOTTLE (70518-0050-1) December 30, 2016
70518-0050-2 70518-0050 REMEDYREPACK INC. 100 TABLET in 1 BOTTLE, PLASTIC (70518-0050-2) February 1, 2017
70518-0050-4 70518-0050 REMEDYREPACK INC. 30 TABLET in 1 BOTTLE, PLASTIC (70518-0050-4) November 3, 2018
70518-0251-1 70518-0251 REMEDYREPACK INC. 90 TABLET in 1 BOTTLE, PLASTIC (70518-0251-1) March 17, 2017
70518-0251-3 70518-0251 REMEDYREPACK INC. 30 TABLET in 1 BLISTER PACK (70518-0251-3) April 10, 2018
70518-2528-1 70518-2528 REMEDYREPACK INC. 30 TABLET in 1 BLISTER PACK (70518-2528-1) August 21, 2025
70518-3061-2 70518-3061 REMEDYREPACK INC. 30 TABLET in 1 BLISTER PACK (70518-3061-2) November 29, 2023
70518-3061-6 70518-3061 REMEDYREPACK INC. 50 POUCH in 1 BOX (70518-3061-6) / 1 TABLET in 1 POUCH (70518-3061-7) April 23, 2026
70518-3757-0 70518-3757 REMEDYREPACK INC. 30 TABLET in 1 BLISTER PACK (70518-3757-0) June 11, 2023
70518-4609-0 70518-4609 REMEDYREPACK INC. 50 POUCH in 1 BOX (70518-4609-0) / 1 TABLET in 1 POUCH (70518-4609-1) April 23, 2026
70518-4679-0 70518-4679 REMEDYREPACK INC. 30 TABLET in 1 BLISTER PACK (70518-4679-0) June 22, 2026
67296-2136-1 67296-2136 Redpharm Drug 3 TABLET in 1 BOTTLE (67296-2136-1) November 5, 2022
67296-2136-2 67296-2136 Redpharm Drug 6 TABLET in 1 BOTTLE (67296-2136-2) November 5, 2022
67296-2136-3 67296-2136 Redpharm Drug 30 TABLET in 1 BOTTLE (67296-2136-3) November 5, 2022
67296-2136-4 67296-2136 Redpharm Drug 7 TABLET in 1 BOTTLE (67296-2136-4) November 5, 2022
67296-2136-5 67296-2136 Redpharm Drug 5 TABLET in 1 BOTTLE (67296-2136-5) November 5, 2022
67296-2136-6 67296-2136 Redpharm Drug 10 TABLET in 1 BOTTLE (67296-2136-6) November 5, 2022
67296-2139-3 67296-2139 Redpharm Drug 30 TABLET in 1 BOTTLE (67296-2139-3) November 5, 2022
64980-562-01 64980-562 Rising Pharma Holdings, Inc. 100 TABLET in 1 BOTTLE (64980-562-01) November 5, 2022
64980-562-10 64980-562 Rising Pharma Holdings, Inc. 1000 TABLET in 1 BOTTLE (64980-562-10) November 5, 2022
64980-563-01 64980-563 Rising Pharma Holdings, Inc. 100 TABLET in 1 BOTTLE (64980-563-01) November 5, 2022
64980-563-10 64980-563 Rising Pharma Holdings, Inc. 1000 TABLET in 1 BOTTLE (64980-563-10) November 5, 2022
64980-564-01 64980-564 Rising Pharma Holdings, Inc. 100 TABLET in 1 BOTTLE (64980-564-01) November 5, 2022
64980-564-50 64980-564 Rising Pharma Holdings, Inc. 500 TABLET in 1 BOTTLE (64980-564-50) November 5, 2022
43547-401-10 43547-401 Solco Healthcare LLC 100 TABLET in 1 BOTTLE, PLASTIC (43547-401-10) March 26, 2004
43547-401-11 43547-401 Solco Healthcare LLC 1000 TABLET in 1 BOTTLE, PLASTIC (43547-401-11) March 26, 2004
43547-401-51 43547-401 Solco Healthcare LLC 5000 TABLET in 1 BOTTLE, PLASTIC (43547-401-51) March 26, 2004
43547-401-94 43547-401 Solco Healthcare LLC 2000000 TABLET in 1 DRUM (43547-401-94) January 1, 2022
43547-402-10 43547-402 Solco Healthcare LLC 100 TABLET in 1 BOTTLE, PLASTIC (43547-402-10) March 26, 2004
43547-402-11 43547-402 Solco Healthcare LLC 1000 TABLET in 1 BOTTLE, PLASTIC (43547-402-11) March 26, 2004
43547-402-51 43547-402 Solco Healthcare LLC 5000 TABLET in 1 BOTTLE, PLASTIC (43547-402-51) March 26, 2004
43547-402-94 43547-402 Solco Healthcare LLC 1000000 TABLET in 1 DRUM (43547-402-94) January 1, 2022
43547-403-10 43547-403 Solco Healthcare LLC 100 TABLET in 1 BOTTLE, PLASTIC (43547-403-10) March 26, 2004
43547-403-11 43547-403 Solco Healthcare LLC 1000 TABLET in 1 BOTTLE, PLASTIC (43547-403-11) March 26, 2004
43547-403-50 43547-403 Solco Healthcare LLC 500 TABLET in 1 BOTTLE, PLASTIC (43547-403-50) March 26, 2004
43547-403-94 43547-403 Solco Healthcare LLC 500000 TABLET in 1 DRUM (43547-403-94) January 1, 2022
60760-858-90 60760-858 St. Mary's Medical Park Pharmacy 90 TABLET in 1 BOTTLE, PLASTIC (60760-858-90) June 15, 2023
87441-033-01 87441-033 Unit Dose Solutions, Inc. 30 TABLET in 1 BLISTER PACK (87441-033-01) June 22, 2026
50090-2713 50090-2713 A-S Medication Solutions — February 1, 2006
50090-3313 50090-3313 A-S Medication Solutions — February 1, 2006
50090-5429 50090-5429 A-S Medication Solutions — February 1, 2006
50090-5702 50090-5702 A-S Medication Solutions — February 1, 2006
50090-6219 50090-6219 A-S Medication Solutions — November 10, 1983
50090-6642 50090-6642 A-S Medication Solutions — November 5, 2022
50090-6646 50090-6646 A-S Medication Solutions — November 5, 2022
50090-6647 50090-6647 A-S Medication Solutions — November 5, 2022
50090-6937 50090-6937 A-S Medication Solutions — February 1, 2006
50090-6942 50090-6942 A-S Medication Solutions — November 5, 2022
50090-7703 50090-7703 A-S Medication Solutions — June 3, 2024
50090-7704 50090-7704 A-S Medication Solutions — June 3, 2024
50090-7705 50090-7705 A-S Medication Solutions — June 3, 2024
50090-7706 50090-7706 A-S Medication Solutions — June 3, 2024
50090-7708 50090-7708 A-S Medication Solutions — June 3, 2024
43353-069 43353-069 Aphena Pharma Solutions - Tennessee, LLC — November 10, 1983
43353-747 43353-747 Aphena Pharma Solutions - Tennessee, LLC — November 10, 1983
71610-049 71610-049 Aphena Pharma Solutions - Tennessee, LLC — March 26, 2004
71610-096 71610-096 Aphena Pharma Solutions - Tennessee, LLC — March 26, 2004
71610-634 71610-634 Aphena Pharma Solutions - Tennessee, LLC — January 4, 2022
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63629-1215 63629-1215 Bryant Ranch Prepack — March 26, 2004
63629-1216 63629-1216 Bryant Ranch Prepack — March 26, 2004
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71335-0384 71335-0384 Bryant Ranch Prepack — February 1, 2006
71335-0842 71335-0842 Bryant Ranch Prepack — March 26, 2004
71335-0852 71335-0852 Bryant Ranch Prepack — March 26, 2004
71335-2317 71335-2317 Bryant Ranch Prepack — November 5, 2022
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72162-1360 72162-1360 Bryant Ranch Prepack — March 26, 2004
72162-1361 72162-1361 Bryant Ranch Prepack — March 26, 2004
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Sources for this page

Every dataset that contributed a fact to this page.
Dataset Agency Used for
NDC Directory FDA Identity, ingredients, strengths, forms, routes, labelers, packages
Drugs@FDA FDA Application, sponsor, submissions, review documents, marketing status
Orange Book FDA Therapeutic equivalence codes, reference drug flags, patents, exclusivity
Drug Labeling FDA / NLM Prescribing information reproduced above
FAERS FDA Adverse event report counts
Enforcement FDA Recall records

Generated September 25, 2026 · 13 sections on this page.