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Penicillin V Potassium

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
Penicillin V Potassium
Generic name
Penicillin V Potassium
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA
Labeler
PD-Rx Pharmaceuticals, Inc.
Product type
Human Prescription Drug
DEA schedule
Not scheduled
Active ingredients
2
NDC product codes
57
Packages
143
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
Penicillin V Potassium 250 mg/1 834040 View
Penicillin V Potassium 500 mg/1 834040 View

Forms, strengths and routes

Source: NDC Directory
Dosage form
Tablet, Film Coated
Route of administration
Oral
Presentations
200

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
Penicillin-class Antibacterial [EPC] EPC All 38 members
Penicillins [CS] CS All 38 members

Regulatory status

Source: Drugs@FDANDC Directory
Application number
065435
Application type
ANDA · Abbreviated New Drug Application
Approval date
April 29, 2008
Sponsor
AUROBINDO PHARMA
Products on application
2
Submissions recorded
2
Products approved under application 065435.
Product Trade name Form Strength Ingredient Status TE Flags
065435-001 PENICILLIN V POTASSIUM TABLET PENICILLIN V POTASSIUM Prescription AB
065435-002 PENICILLIN V POTASSIUM TABLET PENICILLIN V POTASSIUM Prescription AB RS

Therapeutic equivalence

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

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 065435.
Type No. Action Status Date Review
Supplement 5 Labeling Approved August 5, 2014 Standard
Original application 1 Approved April 29, 2008 —

Prescribing information

Source: openFDA Drug Labeling

Reproduced verbatim from the Structured Product Labeling submitted to the FDA (effective 20260728). This is the manufacturer's labelling text, not a summary and not advice.

HUMAN PRESCRIPTION DRUG · 20260728 HUMAN PRESCRIPTION DRUG · 20260728 HUMAN PRESCRIPTION DRUG · 20260601 HUMAN PRESCRIPTION DRUG · 20250204

Indications and Usage

openFDA Drug Labeling

INDICATIONS AND USAGE Penicillin V Potassium Tablets are indicated in the treatment of mild to moderately severe infections due to penicillin G-sensitive microorganisms. Therapy should be guided by bacteriological studies (including sensitivity tests) and by clinical response. NOTE: Severe pneumonia, empyema, bacteremia, pericarditis, meningitis, and arthritis should not be treated with penicillin V during the acute stage. Indicated surgical procedures should be performed. The following infections will usually respond to adequate dosage of penicillin V. Streptococcal Infections (without bacteremia) Mild-to-moderate infections of the upper respiratory tract, scarlet fever, and mild erysipelas. NOTE: Streptococci in groups A, C, G, H, L, and M are very sensitive to penicillin. Other groups, including group D (enterococcus), are resistant. Pneumococcal Infections Mild to moderately severe infections of the respiratory tract. Staphylococcal infections – penicillin G-sensitive Mild infections of the skin and soft tissues. NOTE: Reports indicate an increasing number of strains of staphylococci resistant to penicillin G, emphasizing the need for culture and sensitivity studies in treating suspected staphylococcal infections. Fusospirochetosis (Vincent's gingivitis and pharyngitis) Mild to moderately severe infections of the oropharynx usually respond to therapy with oral penicillin. NOTE: Necessary dental care should be accomplished in infections involving the gum tissue. Medical conditions in which oral penicillin therapy is indicated as prophylaxis: For the prevention of recurrence following rheumatic fever and/or chorea: Prophylaxis with oral penicillin on a continuing basis has proven effective in preventing recurrence of these conditions. Although no controlled clinical efficacy studies have been conducted, penicillin V has been suggested by the American Heart Association and the American Dental Association for use as an oral regimen for prophylaxis against bacterial endocarditis in patients who have congenital heart disease or rheumatic or other acquired valvular heart disease when they undergo dental procedures and surgical procedures of the upper respiratory tract 1 . Oral penicillin should not be used in those patients at particularly high risk for endocarditis (e.g., those with prosthetic heart valves or surgically constructed systemic pulmonary shunts). Penicillin V should not be used as adjunctive prophylaxis for genitourinary instrumentation or surgery, lower-intestinal tract surgery, sigmoidoscopy, and childbirth. Since it may happen that alpha hemolytic streptococci relatively resistant to penicillin may be found when patients are receiving continuous oral penicillin for secondary prevention of rheumatic fever, prophylactic agents other than penicillin may be chosen for these patients and prescribed in addition to their continuous rheumatic fever prophylactic regimen. NOTE: When selecting antibiotics for the prevention of bacterial endocarditis, the physician or dentist should read the full joint statement of the American Heart Association and the American Dental Association 1 . To reduce the development of drug-resistant bacteria and maintain the effectiveness of Penicillin V Potassium Tablets and other antibacterial drugs, Penicillin V Potassium Tablets should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Dosage and Administration

openFDA Drug Labeling

DOSAGE AND ADMINISTRATION The dosage of penicillin V potassium tablets should be determined according to the sensitivity of the causative microorganisms and the severity of infection, and adjusted to the clinical response of the patient. The usual dosage recommendations for adults and children 12 years and over are as follows: Streptococcal Infections Mild to moderately severe - of the upper respiratory tract and including scarlet fever and erysipelas: 125 to 250 mg (200,000 to 400,000 units) every 6 to 8 hours for 10 days. Pneumococcal Infections Mild to moderately severe - of the respiratory tract, including otitis media: 250 to 500 mg (400,000 to 800,000 units) every 6 hours until the patient has been afebrile for at least 2 days. Staphylococcal Infections Mild infections of skin and soft tissue (culture and sensitive tests should be performed): 250 to 500 mg (400,000 to 800,000 units) every 6 to 8 hours. Fusospirochetosis (Vincent's infection) of the oropharynx. Mild to moderately severe infections: 250 to 500 mg (400,000 to 800,000 units) every 6 to 8 hours. For the prevention of recurrence following rheumatic fever and/or chorea: 125 to 250 mg (200,000 to 400,000 units) twice daily on a continuing basis. For prophylaxis against bacterial endocarditis 1 in patients with congenital heart disease or rheumatic or other acquired valvular heart disease when undergoing dental procedures or surgical procedures of the upper respiratory tract: 2 gram of penicillin V (1 gram for children under 60 lbs.) 1 hour before the procedure, and then, 1 gram (500 mg for children under 60 lbs.) 6 hours later.

Contraindications

openFDA Drug Labeling

Contraindications Section A previous hypersensitivity reaction to any penicillin is a contraindication.

Warnings Section SERIOUS AND OCCASIONALLY FATAL HYPERSENSITIVITY (anaphylactic) REACTIONS HAVE BEEN REPORTED IN PATIENTS ON PENICILLIN THERAPY. THESE REACTIONS ARE MORE LIKELY TO OCCUR IN INDIVIDUALS WITH A HISTORY OF PENICILLIN HYPERSENSITIVITY AND/OR A HISTORY OF SENSITIVITY TO MULTIPLE ALLERGENS. THERE HAVE BEEN REPORTS OF INDIVIDUALS WITH A HISTORY OF PENICILLIN HYPERSENSITIVITY WHO HAVE EXPERIENCED SEVERE REACTIONS WHEN TREATED WITH CEPHALOSPORINS. BEFORE INITIATING THERAPY WITH PENICILLIN V POTASSIUM TABLETS, CAREFUL INQUIRY SHOULD BE MADE CONCERNING PREVIOUS HYPERSENSITIVITY REACTIONS TO PENICILLINS, CEPHALOSPORINS, OR OTHER ALLERGENS. IF AN ALLERGIC REACTION OCCURS, PENICILLIN V POTASSIUM TABLETS SHOULD BE DISCONTINUED AND APPROPRIATE THERAPY INSTITUTED. SERIOUS ANAPHYLACTIC REACTIONS REQUIRE IMMEDIATE EMERGENCY TREATMENT WITH EPINEPHRINE. OXYGEN, INTRAVENOUS STEROIDS, AND AIRWAY MANAGEMENT, INCLUDING INTUBATION, SHOULD ALSO BE ADMINISTERED AS INDICATED. Clostridium difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including penicillin V potassium tablets, and may range in severity from mild diarrhea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile . C. difficile produces toxins A and B which contribute to the development of CDAD. Hypertoxin producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea following antibiotic use. Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents. If CDAD is suspected or confirmed, ongoing antibiotic use not directed against C. difficile may need to be discontinued. Appropriate fluid and electrolyte management, protein supplementation, antibiotic treatment of C. difficile , and surgical evaluation should be instituted as clinically indicated.

Adverse Reactions

openFDA Drug Labeling

ADVERSE REACTIONS Although the incidence of reactions to oral penicillins has been reported with much less frequency than following parenteral therapy, it should be remembered that all degrees of hypersensitivity, including fatal anaphylaxis, have been reported with oral penicillin. The most common reactions to oral penicillin are nausea, vomiting, epigastric distress, diarrhea, and black hairy tongue. The hypersensitivity reactions reported are skin eruptions (maculopapular to exfoliative dermatitis), urticaria and other serum-sicknesslike reactions, laryngeal edema, and anaphylaxis. Fever and eosinophilia may frequently be the only reaction observed. Hemolytic anemia, leukopenia, thrombocytopenia, neuropathy, and nephropathy are infrequent reactions and usually associated with high doses of parenteral penicillin. To report SUSPECTED ADVERSE REACTIONS, contact West-Ward Pharmaceuticals Corp. at 1-877-233-2001, or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

Description

openFDA Drug Labeling

DESCRIPTION Penicillin V is the phenoxymethyl analog of penicillin G. Penicillin V potassium is the potassium salt of penicillin V. Penicillin V potassium tablets, for oral administration, contain 250 mg (400,000 units) or 500 mg (800,000 units). The 250 mg tablet is equivalent to 250 mg (400,000 units) penicillin V and the 500 mg tablet is equivalent to 500 mg (800,000 units) penicillin V. In addition, each tablet contains the following inactive ingredients: povidone, microcrystalline cellulose, talc, colloidal silicon dioxide, magnesium stearate, hypromellose, polyethylene glycol, and titanium dioxide. Chemical Structure

How Supplied / Storage and Handling

openFDA Drug Labeling

HOW SUPPLIED Penicillin V Potassium Tablets USP, 500 mg (800,000 units)are white to off-white, capsule shaped, film-coated tablets, debossed with 'E' and a break line on one side and '8' and '5' separated with a break line on the other side. NDC: 70518-2758-00 NDC: 70518-2758-01 NDC: 70518-2758-02 NDC: 70518-2758-03 NDC: 70518-2758-04 NDC: 70518-2758-05 NDC: 70518-2758-06 NDC: 70518-2758-07 NDC: 70518-2758-08 NDC: 70518-2758-09 PACKAGING: 30 in 1 BLISTER PACK PACKAGING: 28 in 1 BLISTER PACK PACKAGING: 20 in 1 BOTTLE, PLASTIC PACKAGING: 20 in 1 BOTTLE, PLASTIC PACKAGING: 14 in 1 BOTTLE, PLASTIC PACKAGING: 100 in 1 BOX PACKAGING: 1 in 1 POUCH PACKAGING: 30 in 1 BOTTLE PLASTIC PACKAGING; 28 in 1 BOTTLE PLASTIC PACKAGING; 28 in 1 BOTTLE PLASTIC Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature]. Dispense in a tight container, as defined in the USP. Keep tightly closed. Keep out of reach of children. Repackaged and Distributed By: Remedy Repack, Inc. 625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762

Adverse event reports

Source: openFDA FAERS
2,540
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: PENICILLIN V POTASSIUM. 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 III April 19, 2017 Citron Pharma Llc Presence of Foreign Tablet/Capsule; Amoxicillin 500 mg was found in bottles of Penicillin V potassium 500 mg Terminated

Packaging and NDCs

Source: NDC Directory
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
50090-3307-0 50090-3307 A-S Medication Solutions 40 TABLET, FILM COATED in 1 BOTTLE (50090-3307-0) December 19, 2017
50090-3307-1 50090-3307 A-S Medication Solutions 28 TABLET, FILM COATED in 1 BOTTLE (50090-3307-1) October 31, 2023
50090-3374-0 50090-3374 A-S Medication Solutions 20 TABLET, FILM COATED in 1 BOTTLE (50090-3374-0) October 8, 2018
50090-3374-2 50090-3374 A-S Medication Solutions 28 TABLET, FILM COATED in 1 BOTTLE (50090-3374-2) April 5, 2018
50090-3374-3 50090-3374 A-S Medication Solutions 30 TABLET, FILM COATED in 1 BOTTLE (50090-3374-3) April 6, 2018
50090-3374-4 50090-3374 A-S Medication Solutions 40 TABLET, FILM COATED in 1 BOTTLE (50090-3374-4) February 16, 2018
50090-3425-0 50090-3425 A-S Medication Solutions 40 TABLET, FILM COATED in 1 BOTTLE (50090-3425-0) March 30, 2018
50090-3425-1 50090-3425 A-S Medication Solutions 28 TABLET, FILM COATED in 1 BOTTLE (50090-3425-1) February 5, 2024
50090-3506-0 50090-3506 A-S Medication Solutions 20 TABLET, FILM COATED in 1 BOTTLE (50090-3506-0) October 8, 2018
50090-3506-2 50090-3506 A-S Medication Solutions 28 TABLET, FILM COATED in 1 BOTTLE (50090-3506-2) July 18, 2018
50090-3506-3 50090-3506 A-S Medication Solutions 30 TABLET, FILM COATED in 1 BOTTLE (50090-3506-3) February 16, 2024
50090-3506-4 50090-3506 A-S Medication Solutions 40 TABLET, FILM COATED in 1 BOTTLE (50090-3506-4) February 16, 2024
50090-4651-0 50090-4651 A-S Medication Solutions 40 TABLET, FILM COATED in 1 BOTTLE (50090-4651-0) October 25, 2019
50090-4651-1 50090-4651 A-S Medication Solutions 28 TABLET, FILM COATED in 1 BOTTLE (50090-4651-1) October 31, 2023
50090-4652-1 50090-4652 A-S Medication Solutions 12 TABLET, FILM COATED in 1 BOTTLE (50090-4652-1) October 25, 2019
50090-4652-2 50090-4652 A-S Medication Solutions 20 TABLET, FILM COATED in 1 BOTTLE (50090-4652-2) October 25, 2019
50090-4652-4 50090-4652 A-S Medication Solutions 28 TABLET, FILM COATED in 1 BOTTLE (50090-4652-4) October 25, 2019
50090-4652-5 50090-4652 A-S Medication Solutions 30 TABLET, FILM COATED in 1 BOTTLE (50090-4652-5) October 25, 2019
50090-4652-6 50090-4652 A-S Medication Solutions 40 TABLET, FILM COATED in 1 BOTTLE (50090-4652-6) October 25, 2019
50090-5543-0 50090-5543 A-S Medication Solutions 6 TABLET, FILM COATED in 1 BOTTLE (50090-5543-0) May 14, 2021
50090-5543-1 50090-5543 A-S Medication Solutions 12 TABLET, FILM COATED in 1 BOTTLE (50090-5543-1) May 14, 2021
50090-5543-2 50090-5543 A-S Medication Solutions 20 TABLET, FILM COATED in 1 BOTTLE (50090-5543-2) January 17, 2023
50090-5543-4 50090-5543 A-S Medication Solutions 28 TABLET, FILM COATED in 1 BOTTLE (50090-5543-4) January 17, 2023
50090-5543-5 50090-5543 A-S Medication Solutions 30 TABLET, FILM COATED in 1 BOTTLE (50090-5543-5) January 17, 2023
50090-5543-6 50090-5543 A-S Medication Solutions 40 TABLET, FILM COATED in 1 BOTTLE (50090-5543-6) May 14, 2021
50090-6675-0 50090-6675 A-S Medication Solutions 40 TABLET, FILM COATED in 1 BOTTLE (50090-6675-0) September 5, 2023
50090-6675-1 50090-6675 A-S Medication Solutions 28 TABLET, FILM COATED in 1 BOTTLE (50090-6675-1) November 14, 2023
65862-175-01 65862-175 Aurobindo Pharma Limited 100 TABLET, FILM COATED in 1 BOTTLE (65862-175-01) April 29, 2008
65862-175-35 65862-175 Aurobindo Pharma Limited 3500 TABLET, FILM COATED in 1 BAG (65862-175-35) April 29, 2008
65862-175-99 65862-175 Aurobindo Pharma Limited 1000 TABLET, FILM COATED in 1 BOTTLE (65862-175-99) April 29, 2008
65862-176-01 65862-176 Aurobindo Pharma Limited 100 TABLET, FILM COATED in 1 BOTTLE (65862-176-01) April 29, 2008
65862-176-05 65862-176 Aurobindo Pharma Limited 500 TABLET, FILM COATED in 1 BOTTLE (65862-176-05) April 29, 2008
65862-176-15 65862-176 Aurobindo Pharma Limited 1500 TABLET, FILM COATED in 1 BAG (65862-176-15) April 29, 2008
65862-176-99 65862-176 Aurobindo Pharma Limited 1000 TABLET, FILM COATED in 1 BOTTLE (65862-176-99) April 29, 2008
63629-5050-1 63629-5050 Bryant Ranch Prepack 40 TABLET, FILM COATED in 1 BOTTLE (63629-5050-1) March 12, 2026
63629-7623-1 63629-7623 Bryant Ranch Prepack 20 TABLET, FILM COATED in 1 BOTTLE (63629-7623-1) November 4, 2021
63629-7928-1 63629-7928 Bryant Ranch Prepack 40 TABLET, FILM COATED in 1 BOTTLE (63629-7928-1) June 17, 2022
63629-9110-1 63629-9110 Bryant Ranch Prepack 30 TABLET, FILM COATED in 1 BOTTLE (63629-9110-1) March 16, 2023
71335-2702-1 71335-2702 Bryant Ranch Prepack 40 TABLET, FILM COATED in 1 BOTTLE (71335-2702-1) September 26, 2025
0143-9836-01 0143-9836 Hikma Pharmaceuticals USA Inc. 100 TABLET, FILM COATED in 1 BOTTLE (0143-9836-01) October 11, 2013
0143-9836-10 0143-9836 Hikma Pharmaceuticals USA Inc. 1000 TABLET, FILM COATED in 1 BOTTLE (0143-9836-10) October 11, 2013
0143-9837-01 0143-9837 Hikma Pharmaceuticals USA Inc. 100 TABLET, FILM COATED in 1 BOTTLE (0143-9837-01) October 11, 2013
0143-9837-10 0143-9837 Hikma Pharmaceuticals USA Inc. 1000 TABLET, FILM COATED in 1 BOTTLE (0143-9837-10) October 11, 2013
16714-234-01 16714-234 NorthStar Rx LLC 100 TABLET, FILM COATED in 1 BOTTLE (16714-234-01) April 29, 2008
16714-234-02 16714-234 NorthStar Rx LLC 1000 TABLET, FILM COATED in 1 BOTTLE (16714-234-02) April 29, 2008
16714-235-01 16714-235 NorthStar Rx LLC 100 TABLET, FILM COATED in 1 BOTTLE (16714-235-01) April 29, 2008
16714-235-02 16714-235 NorthStar Rx LLC 1000 TABLET, FILM COATED in 1 BOTTLE (16714-235-02) April 29, 2008
68071-3176-2 68071-3176 NuCare Pharmaceuticals, Inc. 20 TABLET, FILM COATED in 1 BOTTLE (68071-3176-2) March 17, 2017
68071-3176-3 68071-3176 NuCare Pharmaceuticals, Inc. 30 TABLET, FILM COATED in 1 BOTTLE (68071-3176-3) March 17, 2017
68071-3176-4 68071-3176 NuCare Pharmaceuticals, Inc. 40 TABLET, FILM COATED in 1 BOTTLE (68071-3176-4) March 17, 2017
68071-3176-6 68071-3176 NuCare Pharmaceuticals, Inc. 6 TABLET, FILM COATED in 1 BOTTLE (68071-3176-6) March 17, 2017
68071-3176-8 68071-3176 NuCare Pharmaceuticals, Inc. 28 TABLET, FILM COATED in 1 BOTTLE (68071-3176-8) March 17, 2017
68071-3299-4 68071-3299 NuCare Pharmaceuticals,Inc. 4 TABLET, FILM COATED in 1 BOTTLE (68071-3299-4) January 18, 2018
68071-3299-6 68071-3299 NuCare Pharmaceuticals,Inc. 6 TABLET, FILM COATED in 1 BOTTLE (68071-3299-6) January 18, 2018
68071-3299-9 68071-3299 NuCare Pharmaceuticals,Inc. 9 TABLET, FILM COATED in 1 BOTTLE (68071-3299-9) January 18, 2018
68071-3401-4 68071-3401 NuCare Pharmaceuticals,Inc. 40 TABLET, FILM COATED in 1 BOTTLE (68071-3401-4) May 16, 2023
68071-3427-6 68071-3427 NuCare Pharmaceuticals,Inc. 6 TABLET, FILM COATED in 1 BOTTLE (68071-3427-6) June 6, 2023
68071-3562-4 68071-3562 NuCare Pharmaceuticals,Inc. 40 TABLET, FILM COATED in 1 BOTTLE (68071-3562-4) January 24, 2024
68071-3640-3 68071-3640 NuCare Pharmaceuticals,Inc. 30 TABLET, FILM COATED in 1 BOTTLE (68071-3640-3) July 2, 2024
68071-3640-4 68071-3640 NuCare Pharmaceuticals,Inc. 40 TABLET, FILM COATED in 1 BOTTLE (68071-3640-4) February 28, 2025
68071-3640-8 68071-3640 NuCare Pharmaceuticals,Inc. 28 TABLET, FILM COATED in 1 BOTTLE (68071-3640-8) April 23, 2025
68071-4298-3 68071-4298 NuCare Pharmaceuticals,Inc. 3 TABLET, FILM COATED in 1 BOTTLE (68071-4298-3) December 6, 2024
68071-4298-4 68071-4298 NuCare Pharmaceuticals,Inc. 4 TABLET, FILM COATED in 1 BOTTLE (68071-4298-4) February 23, 2018
68071-4298-6 68071-4298 NuCare Pharmaceuticals,Inc. 6 TABLET, FILM COATED in 1 BOTTLE (68071-4298-6) February 23, 2018
68071-4298-8 68071-4298 NuCare Pharmaceuticals,Inc. 8 TABLET, FILM COATED in 1 BOTTLE (68071-4298-8) February 23, 2018
68071-4298-9 68071-4298 NuCare Pharmaceuticals,Inc. 9 TABLET, FILM COATED in 1 BOTTLE (68071-4298-9) February 23, 2018
68071-4697-4 68071-4697 NuCare Pharmaceuticals,Inc. 40 TABLET, FILM COATED in 1 BOTTLE (68071-4697-4) January 7, 2019
68071-4697-8 68071-4697 NuCare Pharmaceuticals,Inc. 28 TABLET, FILM COATED in 1 BOTTLE (68071-4697-8) January 7, 2019
68071-4753-6 68071-4753 NuCare Pharmaceuticals,Inc. 6 TABLET, FILM COATED in 1 BOTTLE (68071-4753-6) February 6, 2019
68071-4753-8 68071-4753 NuCare Pharmaceuticals,Inc. 8 TABLET, FILM COATED in 1 BOTTLE (68071-4753-8) February 6, 2019
68071-4838-2 68071-4838 NuCare Pharmaceuticals,Inc. 20 TABLET, FILM COATED in 1 BOTTLE (68071-4838-2) August 21, 2026
68071-4838-3 68071-4838 NuCare Pharmaceuticals,Inc. 30 TABLET, FILM COATED in 1 BOTTLE (68071-4838-3) April 9, 2019
68071-4838-8 68071-4838 NuCare Pharmaceuticals,Inc. 28 TABLET, FILM COATED in 1 BOTTLE (68071-4838-8) April 9, 2019
68071-5081-6 68071-5081 NuCare Pharmaceuticals,Inc. 6 TABLET, FILM COATED in 1 BOTTLE (68071-5081-6) October 8, 2019
43063-557-04 43063-557 PD-Rx Pharmaceuticals, Inc. 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-557-04) December 13, 2016
43063-557-06 43063-557 PD-Rx Pharmaceuticals, Inc. 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-557-06) December 13, 2016
43063-557-15 43063-557 PD-Rx Pharmaceuticals, Inc. 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-557-15) October 24, 2016
43063-557-20 43063-557 PD-Rx Pharmaceuticals, Inc. 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-557-20) September 13, 2016
43063-557-28 43063-557 PD-Rx Pharmaceuticals, Inc. 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-557-28) January 23, 2015
43063-557-30 43063-557 PD-Rx Pharmaceuticals, Inc. 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-557-30) August 24, 2016
43063-557-40 43063-557 PD-Rx Pharmaceuticals, Inc. 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-557-40) March 18, 2015
43063-576-28 43063-576 PD-Rx Pharmaceuticals, Inc. 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-576-28) June 26, 2015
43063-576-40 43063-576 PD-Rx Pharmaceuticals, Inc. 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-576-40) June 26, 2015
43063-614-40 43063-614 PD-Rx Pharmaceuticals, Inc. 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-614-40) September 14, 2015
43063-622-40 43063-622 PD-Rx Pharmaceuticals, Inc. 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-622-40) October 26, 2015
43063-680-40 43063-680 PD-Rx Pharmaceuticals, Inc. 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-680-40) June 17, 2016
43063-704-06 43063-704 PD-Rx Pharmaceuticals, Inc. 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-704-06) November 2, 2016
43063-704-20 43063-704 PD-Rx Pharmaceuticals, Inc. 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-704-20) September 19, 2016
43063-704-28 43063-704 PD-Rx Pharmaceuticals, Inc. 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-704-28) August 22, 2016
43063-704-40 43063-704 PD-Rx Pharmaceuticals, Inc. 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-704-40) December 15, 2016
43063-780-06 43063-780 PD-Rx Pharmaceuticals, Inc. 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-780-06) August 4, 2020
43063-780-15 43063-780 PD-Rx Pharmaceuticals, Inc. 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-780-15) September 1, 2017
43063-780-20 43063-780 PD-Rx Pharmaceuticals, Inc. 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-780-20) September 27, 2017
43063-780-28 43063-780 PD-Rx Pharmaceuticals, Inc. 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-780-28) March 5, 2018
43063-780-30 43063-780 PD-Rx Pharmaceuticals, Inc. 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-780-30) August 7, 2018
43063-780-40 43063-780 PD-Rx Pharmaceuticals, Inc. 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-780-40) August 7, 2018
43063-995-28 43063-995 PD-Rx Pharmaceuticals, Inc. 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-995-28) December 11, 2023
43063-995-40 43063-995 PD-Rx Pharmaceuticals, Inc. 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-995-40) July 24, 2019
72789-146-06 72789-146 PD-Rx Pharmaceuticals, Inc. 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-146-06) December 30, 2020
72789-146-20 72789-146 PD-Rx Pharmaceuticals, Inc. 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-146-20) December 30, 2020
72789-146-28 72789-146 PD-Rx Pharmaceuticals, Inc. 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-146-28) March 15, 2021
72789-222-01 72789-222 PD-Rx Pharmaceuticals, Inc. 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-222-01) October 24, 2022
72789-222-30 72789-222 PD-Rx Pharmaceuticals, Inc. 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-222-30) April 1, 2024
72789-223-01 72789-223 PD-Rx Pharmaceuticals, Inc. 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-223-01) February 11, 2022
72789-245-20 72789-245 PD-Rx Pharmaceuticals, Inc. 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-245-20) April 18, 2025
72789-245-28 72789-245 PD-Rx Pharmaceuticals, Inc. 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-245-28) October 11, 2023
72789-245-40 72789-245 PD-Rx Pharmaceuticals, Inc. 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-245-40) April 12, 2022
72789-366-28 72789-366 PD-Rx Pharmaceuticals, Inc. 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-366-28) December 11, 2023
68788-8242-2 68788-8242 Preferred Pharmaceuticals Inc. 28 TABLET, FILM COATED in 1 BOTTLE (68788-8242-2) August 9, 2022
68788-8242-4 68788-8242 Preferred Pharmaceuticals Inc. 40 TABLET, FILM COATED in 1 BOTTLE (68788-8242-4) August 9, 2022
63187-676-20 63187-676 Proficient Rx LP 20 TABLET, FILM COATED in 1 BOTTLE (63187-676-20) April 1, 2016
63187-676-30 63187-676 Proficient Rx LP 30 TABLET, FILM COATED in 1 BOTTLE (63187-676-30) April 1, 2016
63187-676-40 63187-676 Proficient Rx LP 40 TABLET, FILM COATED in 1 BOTTLE (63187-676-40) April 1, 2016
63187-756-20 63187-756 Proficient Rx LP 20 TABLET, FILM COATED in 1 BOTTLE (63187-756-20) November 1, 2016
63187-756-30 63187-756 Proficient Rx LP 30 TABLET, FILM COATED in 1 BOTTLE (63187-756-30) November 1, 2016
63187-756-40 63187-756 Proficient Rx LP 40 TABLET, FILM COATED in 1 BOTTLE (63187-756-40) November 1, 2016
63187-926-20 63187-926 Proficient Rx LP 20 TABLET, FILM COATED in 1 BOTTLE (63187-926-20) December 1, 2017
63187-926-30 63187-926 Proficient Rx LP 30 TABLET, FILM COATED in 1 BOTTLE (63187-926-30) December 1, 2017
63187-926-40 63187-926 Proficient Rx LP 40 TABLET, FILM COATED in 1 BOTTLE (63187-926-40) December 1, 2017
42708-098-14 42708-098 QPharma Inc 14 TABLET, FILM COATED in 1 BOTTLE (42708-098-14) March 20, 2019
70518-2758-0 70518-2758 REMEDYREPACK INC. 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2758-0) May 28, 2020
70518-2758-1 70518-2758 REMEDYREPACK INC. 28 TABLET, FILM COATED in 1 BLISTER PACK (70518-2758-1) May 28, 2020
70518-2758-2 70518-2758 REMEDYREPACK INC. 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2758-2) November 9, 2021
70518-2758-7 70518-2758 REMEDYREPACK INC. 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2758-7) August 29, 2025
70518-2758-8 70518-2758 REMEDYREPACK INC. 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2758-8) November 24, 2025
70518-2758-9 70518-2758 REMEDYREPACK INC. 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2758-9) May 5, 2026
70518-2808-1 70518-2808 REMEDYREPACK INC. 100 POUCH in 1 BOX (70518-2808-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2808-2) July 24, 2026
70518-2877-2 70518-2877 REMEDYREPACK INC. 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2877-2) August 4, 2026
70518-2877-3 70518-2877 REMEDYREPACK INC. 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2877-3) August 20, 2026
70518-2877-4 70518-2877 REMEDYREPACK INC. 28 TABLET, FILM COATED in 1 BLISTER PACK (70518-2877-4) September 21, 2026
70518-3441-2 70518-3441 REMEDYREPACK INC. 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3441-2) August 21, 2023
70518-3441-5 70518-3441 REMEDYREPACK INC. 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3441-5) June 20, 2025
70518-4657-0 70518-4657 REMEDYREPACK INC. 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4657-0) May 12, 2026
70518-4657-1 70518-4657 REMEDYREPACK INC. 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4657-1) July 28, 2026
67296-2261-2 67296-2261 Redpharm Drug 20 TABLET, FILM COATED in 1 BOTTLE (67296-2261-2) April 29, 2008
67296-2261-3 67296-2261 Redpharm Drug 30 TABLET, FILM COATED in 1 BOTTLE (67296-2261-3) April 29, 2008
67296-2261-4 67296-2261 Redpharm Drug 40 TABLET, FILM COATED in 1 BOTTLE (67296-2261-4) April 29, 2008
67296-2308-4 67296-2308 Redpharm Drug 40 TABLET, FILM COATED in 1 BOTTLE (67296-2308-4) April 29, 2008
57237-040-01 57237-040 Rising Health, LLC 100 TABLET, FILM COATED in 1 BOTTLE (57237-040-01) April 29, 2008
57237-040-99 57237-040 Rising Health, LLC 1000 TABLET, FILM COATED in 1 BOTTLE (57237-040-99) April 29, 2008
57237-041-01 57237-041 Rising Health, LLC 100 TABLET, FILM COATED in 1 BOTTLE (57237-041-01) April 29, 2008
57237-041-05 57237-041 Rising Health, LLC 500 TABLET, FILM COATED in 1 BOTTLE (57237-041-05) April 29, 2008
57237-041-99 57237-041 Rising Health, LLC 1000 TABLET, FILM COATED in 1 BOTTLE (57237-041-99) April 29, 2008
50090-3307 50090-3307 A-S Medication Solutions — October 11, 2013
50090-3374 50090-3374 A-S Medication Solutions — October 11, 2013
50090-3425 50090-3425 A-S Medication Solutions — April 29, 2008
50090-3506 50090-3506 A-S Medication Solutions — April 29, 2008
50090-4651 50090-4651 A-S Medication Solutions — April 29, 2008
50090-4652 50090-4652 A-S Medication Solutions — April 29, 2008
50090-5543 50090-5543 A-S Medication Solutions — April 29, 2008
50090-6675 50090-6675 A-S Medication Solutions — April 29, 2008
65862-175 65862-175 Aurobindo Pharma Limited — April 29, 2008
65862-176 65862-176 Aurobindo Pharma Limited — April 29, 2008
63629-5050 63629-5050 Bryant Ranch Prepack — October 11, 2013
63629-7623 63629-7623 Bryant Ranch Prepack — April 29, 2008
63629-7928 63629-7928 Bryant Ranch Prepack — April 29, 2008
63629-9110 63629-9110 Bryant Ranch Prepack — April 29, 2008
71335-2702 71335-2702 Bryant Ranch Prepack — October 11, 2013
0143-9836 0143-9836 Hikma Pharmaceuticals USA Inc. — October 11, 2013
0143-9837 0143-9837 Hikma Pharmaceuticals USA Inc. — October 11, 2013
16714-234 16714-234 NorthStar Rx LLC — April 29, 2008
16714-235 16714-235 NorthStar Rx LLC — April 29, 2008
68071-3176 68071-3176 NuCare Pharmaceuticals, Inc. — April 29, 2008
68071-3299 68071-3299 NuCare Pharmaceuticals,Inc. — April 29, 2008
68071-3401 68071-3401 NuCare Pharmaceuticals,Inc. — October 11, 2013
68071-3427 68071-3427 NuCare Pharmaceuticals,Inc. — April 29, 2008
68071-3562 68071-3562 NuCare Pharmaceuticals,Inc. — April 29, 2008
68071-3640 68071-3640 NuCare Pharmaceuticals,Inc. — April 29, 2008
68071-4298 68071-4298 NuCare Pharmaceuticals,Inc. — April 29, 2008
68071-4697 68071-4697 NuCare Pharmaceuticals,Inc. — April 29, 2008
68071-4753 68071-4753 NuCare Pharmaceuticals,Inc. — April 29, 2008
68071-4838 68071-4838 NuCare Pharmaceuticals,Inc. — April 29, 2008
68071-5081 68071-5081 NuCare Pharmaceuticals,Inc. — April 29, 2008
43063-557 43063-557 PD-Rx Pharmaceuticals, Inc. — April 29, 2008
43063-576 43063-576 PD-Rx Pharmaceuticals, Inc. — April 29, 2008
43063-614 43063-614 PD-Rx Pharmaceuticals, Inc. — April 29, 2008
43063-622 43063-622 PD-Rx Pharmaceuticals, Inc. — April 29, 2008
43063-680 43063-680 PD-Rx Pharmaceuticals, Inc. — April 29, 2008
43063-704 43063-704 PD-Rx Pharmaceuticals, Inc. — April 29, 2008
43063-780 43063-780 PD-Rx Pharmaceuticals, Inc. — October 11, 2013
43063-995 43063-995 PD-Rx Pharmaceuticals, Inc. — October 11, 2013
72789-146 72789-146 PD-Rx Pharmaceuticals, Inc. — April 29, 2008
72789-222 72789-222 PD-Rx Pharmaceuticals, Inc. — October 11, 2013
72789-223 72789-223 PD-Rx Pharmaceuticals, Inc. — October 11, 2013
72789-245 72789-245 PD-Rx Pharmaceuticals, Inc. — October 11, 2013
72789-366 72789-366 PD-Rx Pharmaceuticals, Inc. — October 11, 2013
68788-8242 68788-8242 Preferred Pharmaceuticals Inc. — August 9, 2022
63187-676 63187-676 Proficient Rx LP — April 29, 2008
63187-756 63187-756 Proficient Rx LP — April 29, 2008
63187-926 63187-926 Proficient Rx LP — April 29, 2008
42708-098 42708-098 QPharma Inc — April 29, 2008
70518-2758 70518-2758 REMEDYREPACK INC. — May 28, 2020
70518-2808 70518-2808 REMEDYREPACK INC. — July 8, 2020
70518-2877 70518-2877 REMEDYREPACK INC. — September 10, 2020
70518-3441 70518-3441 REMEDYREPACK INC. — June 22, 2022
70518-4657 70518-4657 REMEDYREPACK INC. — May 12, 2026
67296-2261 67296-2261 Redpharm Drug — April 29, 2008
67296-2308 67296-2308 Redpharm Drug — April 29, 2008
57237-040 57237-040 Rising Health, LLC — April 29, 2008
57237-041 57237-041 Rising Health, LLC — April 29, 2008

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.