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Triamcinolone Acetonide

Prescription Veterinary ANDA TE AT RLD 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
Triamcinolone Acetonide
Generic name
Triamcinolone Acetonide
Dosage form
Ointment
Route
Topical
Marketing category
ANDA · ANDA
Labeler
A-S Medication Solutions
Product type
Human Prescription Drug
DEA schedule
Not scheduled
Active ingredients
4
NDC product codes
54
Packages
83
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
Triamcinolone Acetonide .25 mg/g 1014314 View
Triamcinolone Acetonide .5 mg/g 1014314 View
Triamcinolone Acetonide 1 mg/g 1014314 View
Triamcinolone Acetonide 5 mg/g 1014314 View

Forms, strengths and routes

Source: NDC Directory
Dosage form
Ointment
Route of administration
Topical
Presentations
137

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
Corticosteroid Hormone Receptor Agonists [MoA] MoA All 215 members
Corticosteroid [EPC] EPC All 215 members

Regulatory status

Source: Drugs@FDANDC Directory
Application number
087385
Application type
ANDA · Abbreviated New Drug Application
Approval date
November 5, 1981
Sponsor
PADAGIS US
Products on application
3
Submissions recorded
8
Products approved under application 087385.
Product Trade name Form Strength Ingredient Status TE Flags
087385-001 TRIAMCINOLONE ACETONIDE OINTMENT TRIAMCINOLONE ACETONIDE Prescription AT RLD RS
087385-002 TRIAMCINOLONE ACETONIDE OINTMENT TRIAMCINOLONE ACETONIDE Prescription AT RLD RS
087385-003 TRIAMCINOLONE ACETONIDE OINTMENT TRIAMCINOLONE ACETONIDE Prescription AT RLD RS

Therapeutic equivalence

Source: Orange Book
TE code
AT
Reference Listed Drug
Yes
Reference Standard
Yes

What this rating means: Therapeutically equivalent — bioequivalence demonstrated (topical dermatological products)

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 087385.
Type No. Action Status Date Review
Supplement 15 Manufacturing (CMC) Approved March 26, 1999 —
Supplement 13 Labeling Approved June 14, 1995 —
Supplement 12 Manufacturing (CMC) Approved May 13, 1988 —
Supplement 10 Manufacturing (CMC) Approved September 23, 1986 —
Supplement 9 Manufacturing (CMC) Approved June 9, 1986 —
Supplement 3 Manufacturing (CMC) Approved April 28, 1986 —
Supplement 4 Manufacturing (CMC) Approved July 11, 1984 —
Original application 1 Approved November 5, 1981 —

Prescribing information

Source: openFDA Drug Labeling

Reproduced verbatim from the Structured Product Labeling submitted to the FDA (effective 20260317). This is the manufacturer's labelling text, not a summary and not advice.

HUMAN PRESCRIPTION DRUG · 20260317 HUMAN PRESCRIPTION DRUG · 20241204 HUMAN PRESCRIPTION DRUG · 20230701 HUMAN PRESCRIPTION DRUG · 20230228

Indications and Usage

openFDA Drug Labeling

INDICATIONS AND USAGE Triamcinolone Acetonide 0.05% in Absorbase ® (Triamcinolone Acetonide Ointment, USP) is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses.

Dosage and Administration

openFDA Drug Labeling

DOSAGE AND ADMINISTRATION Apply a thin film of the 0.1% Triamcinolone Acetonide Ointment, as appropriate, to the affected area two to three times daily. Occlusive Dressing Technique Occlusive dressings may be used for the management of psoriasis or other recalcitrant conditions. Apply a thin film of ointment to the lesion, cover with a pliable nonporous film, and seal the edges. If needed, additional moisture may be provided by covering the lesion with a dampened clean cotton cloth before the nonporous film is applied or by briefly wetting the affected area with water immediately prior to applying the medication. The frequency of changing dressings is best determined on an individual basis. It may be convenient to apply Triamcinolone Acetonide Ointment under an occlusive dressing in the evening and to remove the dressing in the morning (i.e., 12-hour occlusion). When utilizing the 12-hour occlusion regimen, additional ointment should be applied, without occlusion, during the day. Reapplication is essential at each dressing change. If an infection develops, the use of occlusive dressings should be discontinued and appropriate antimicrobial therapy instituted.

Occlusive Dressing Technique Occlusive dressings may be used for the management of psoriasis or other recalcitrant conditions. Apply a thin film of ointment to the lesion, cover with a pliable nonporous film, and seal the edges. If needed, additional moisture may be provided by covering the lesion with a dampened clean cotton cloth before the nonporous film is applied or by briefly wetting the affected area with water immediately prior to applying the medication. The frequency of changing dressings is best determined on an individual basis. It may be convenient to apply Triamcinolone Acetonide Ointment under an occlusive dressing in the evening and to remove the dressing in the morning (i.e., 12-hour occlusion). When utilizing the 12-hour occlusion regimen, additional ointment should be applied, without occlusion, during the day. Reapplication is essential at each dressing change. If an infection develops, the use of occlusive dressings should be discontinued and appropriate antimicrobial therapy instituted.

Contraindications

openFDA Drug Labeling

CONTRAINDICATIONS Triamcinolone Acetonide 0.05% in Absorbase ® (Triamcinolone Acetonide Ointment, USP) is contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation.

Adverse Reactions

openFDA Drug Labeling

ADVERSE REACTIONS The following local adverse reactions are reported infrequently with topical corticosteroids, but may occur more frequently with the use of occlusive dressings. These reactions are listed in an approximate decreasing order of occurrence: burning, itching, irritation, dryness, folliculitis, hypertrichosis, acneiform eruptions, hypopigmentation, perioral dermatitis, allergic contact dermatitis, maceration of the skin, secondary infection, skin atrophy, striae, and miliaria. To report SUSPECTED ADVERSE REACTIONS, contact Cosette Pharmaceuticals, Inc. at 1-800-922-1038 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch .

Description

openFDA Drug Labeling

Triamcinolone Acetonide Cream USP contains Triamcinolone Acetonide [Pregna-1,4-diene-3,20-dione, 9-fluoro-11,21-dihydroxy-16,17-[(1-methylethylidene)bis- (oxy)]-, (11β,16α)-], with the empirical formula C24H31FO6 and molecular weight 434.50. CAS 76-25-5. [chemstructure] Triamcinolone Acetonide Cream USP, 0.025% contains: 0.25 mg of Triamcinolone Acetonide per gram in a base containing Emulsifying Wax, Cetyl Alcohol, Isopropyl Palmitate, Sorbitol Solution, Glycerin, Lactic Acid, Benzyl Alcohol and Purified Water. Triamcinolone Acetonide Cream USP, 0.1% contains: 1 mg of Triamcinolone Acetonide per gram in a base containing Emulsifying Wax, Cetyl Alcohol, Isopropyl Palmitate, Sorbitol Solution, Glycerin, Lactic Acid, Benzyl Alcohol and Purified Water. Triamcinolone Acetonide Cream USP, 0.5% contains: 5 mg of Triamcinolone Acetonide per gram in a base containing Emulsifying Wax, Cetyl Alcohol, Isopropyl Palmitate, Sorbitol Solution, Glycerin, Lactic Acid, Benzyl Alcohol and Purified Water.

OVERDOSAGE Topically applied corticosteroids can be absorbed in sufficient amounts to produce systemic effects (see PRECAUTIONS, General ).

How Supplied / Storage and Handling

openFDA Drug Labeling

HOW SUPPLIED Triamcinolone Acetonide Ointment USP, 0.025% is available as follows: 15 gram tubes NDC 33342-331-15 80 gram tubes NDC 33342-331-80 454 g jar NDC 33342-331-54 Triamcinolone Acetonide Ointment USP, 0.1% is available as follows: 15 gram tubes NDC 33342-333-15 80 gram tubes NDC 33342-333-80 454 g jar NDC 33342-333-54 Triamcinolone Acetonide Ointment USP, 0.5% is available as follows: 15 gram tubes NDC 33342-332-15 Storage 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]. Manufactured for: Macleods Pharma USA, Inc. Princeton, NJ 08540 Manufacturer: Macleods Pharmaceuticals Limited At Oxalis Labs Baddi, Himachal Pradesh, INDIA To report SUSPECTED ADVERSE REACTIONS, contact Macleods Pharma USA, Inc.at 1-888-943-3210 or 1-855-926- 3384 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. Revised: July 2023

Adverse event reports

Source: openFDA FAERS
31,697
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: TRIAMCINOLONE ACETONIDE. 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 June 2, 2021 Cardinal Health Inc. CGMP Deviations: Intermittent exposure to temperature excursion during storage. 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
50090-2244-0 50090-2244 A-S Medication Solutions 1 TUBE in 1 CARTON (50090-2244-0) / 80 g in 1 TUBE December 2, 2015
50090-3508-0 50090-3508 A-S Medication Solutions 1 TUBE in 1 CARTON (50090-3508-0) / 80 g in 1 TUBE July 19, 2018
50090-3802-0 50090-3802 A-S Medication Solutions 1 TUBE in 1 CARTON (50090-3802-0) / 15 g in 1 TUBE November 9, 2018
50090-4761-0 50090-4761 A-S Medication Solutions 1 TUBE in 1 CARTON (50090-4761-0) / 15 g in 1 TUBE November 27, 2019
50090-5980-0 50090-5980 A-S Medication Solutions 1 TUBE in 1 CARTON (50090-5980-0) / 15 g in 1 TUBE May 18, 2022
50090-6211-0 50090-6211 A-S Medication Solutions 1 TUBE in 1 CARTON (50090-6211-0) / 15 g in 1 TUBE November 7, 2022
50090-6978-0 50090-6978 A-S Medication Solutions 1 TUBE in 1 CARTON (50090-6978-0) / 15 g in 1 TUBE December 26, 2023
50090-7679-0 50090-7679 A-S Medication Solutions 1 TUBE in 1 CARTON (50090-7679-0) / 15 g in 1 TUBE October 8, 2025
76420-360-80 76420-360 Asclemed USA, Inc. 80 g in 1 TUBE (76420-360-80) May 23, 2025
76420-361-00 76420-361 Asclemed USA, Inc. 454 g in 1 JAR (76420-361-00) May 23, 2025
76420-361-15 76420-361 Asclemed USA, Inc. 15 g in 1 TUBE (76420-361-15) May 23, 2025
76420-361-80 76420-361 Asclemed USA, Inc. 80 g in 1 TUBE (76420-361-80) May 23, 2025
63629-8708-1 63629-8708 Bryant Ranch Prepack 430 g in 1 JAR (63629-8708-1) February 9, 2022
63629-8841-1 63629-8841 Bryant Ranch Prepack 80 g in 1 TUBE (63629-8841-1) September 10, 2021
72162-1429-2 72162-1429 Bryant Ranch Prepack 430 g in 1 JAR (72162-1429-2) June 18, 2024
72162-2335-2 72162-2335 Bryant Ranch Prepack 1 TUBE in 1 CARTON (72162-2335-2) / 15 g in 1 TUBE June 18, 2024
72162-2335-4 72162-2335 Bryant Ranch Prepack 1 TUBE in 1 CARTON (72162-2335-4) / 80 g in 1 TUBE June 18, 2024
72162-2336-2 72162-2336 Bryant Ranch Prepack 1 TUBE in 1 CARTON (72162-2336-2) / 15 g in 1 TUBE June 18, 2024
72162-2336-4 72162-2336 Bryant Ranch Prepack 1 TUBE in 1 CARTON (72162-2336-4) / 80 g in 1 TUBE June 18, 2024
46287-010-11 46287-010 CMP Pharma, Inc. 110 g in 1 JAR (46287-010-11) August 23, 2021
24470-922-15 24470-922 Cintex Services, LLC 430 g in 1 JAR (24470-922-15) November 10, 2020
0713-0228-15 0713-0228 Cosette Pharmaceuticals, Inc. 1 TUBE in 1 CARTON (0713-0228-15) / 15 g in 1 TUBE September 10, 2015
0713-0228-31 0713-0228 Cosette Pharmaceuticals, Inc. 1 TUBE in 1 CARTON (0713-0228-31) / 30 g in 1 TUBE December 6, 2024
0713-0228-80 0713-0228 Cosette Pharmaceuticals, Inc. 1 TUBE in 1 CARTON (0713-0228-80) / 80 g in 1 TUBE September 10, 2015
0713-0229-15 0713-0229 Cosette Pharmaceuticals, Inc. 1 TUBE in 1 CARTON (0713-0229-15) / 15 g in 1 TUBE September 10, 2015
0713-0229-80 0713-0229 Cosette Pharmaceuticals, Inc. 1 TUBE in 1 CARTON (0713-0229-80) / 80 g in 1 TUBE September 10, 2015
61919-619-15 61919-619 DIRECTRX 15 g in 1 TUBE (61919-619-15) February 4, 2021
0168-0005-80 0168-0005 E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC 80 g in 1 TUBE (0168-0005-80) February 14, 1978
0168-0006-15 0168-0006 E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC 15 g in 1 TUBE (0168-0006-15) February 14, 1978
0168-0006-16 0168-0006 E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC 454 g in 1 JAR (0168-0006-16) February 14, 1978
0168-0006-80 0168-0006 E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC 80 g in 1 TUBE (0168-0006-80) February 14, 1978
21922-024-11 21922-024 Encube Ethicals, Inc. 430 g in 1 JAR (21922-024-11) December 2, 2019
21922-063-04 21922-063 Encube Ethicals, Inc. 1 TUBE in 1 CARTON (21922-063-04) / 15 g in 1 TUBE August 1, 2023
21922-063-05 21922-063 Encube Ethicals, Inc. 1 TUBE in 1 CARTON (21922-063-05) / 30 g in 1 TUBE March 18, 2025
21922-063-15 21922-063 Encube Ethicals, Inc. 1 TUBE in 1 CARTON (21922-063-15) / 80 g in 1 TUBE August 1, 2023
21922-063-30 21922-063 Encube Ethicals, Inc. 454 g in 1 JAR (21922-063-30) August 1, 2023
68462-797-17 68462-797 Glenmark Pharmaceuticals Inc., USA 1 TUBE in 1 CARTON (68462-797-17) / 15 g in 1 TUBE August 22, 2017
68462-797-49 68462-797 Glenmark Pharmaceuticals Inc., USA 1 TUBE in 1 CARTON (68462-797-49) / 80 g in 1 TUBE August 22, 2017
68462-797-59 68462-797 Glenmark Pharmaceuticals Inc., USA 454 g in 1 JAR (68462-797-59) August 22, 2017
68462-798-17 68462-798 Glenmark Pharmaceuticals Inc., USA 1 TUBE in 1 CARTON (68462-798-17) / 15 g in 1 TUBE July 22, 2016
33342-331-15 33342-331 Macleods Pharmaceuticals Limited 1 TUBE in 1 CARTON (33342-331-15) / 15 g in 1 TUBE November 23, 2018
33342-331-54 33342-331 Macleods Pharmaceuticals Limited 454 g in 1 JAR (33342-331-54) November 23, 2018
33342-331-80 33342-331 Macleods Pharmaceuticals Limited 1 TUBE in 1 CARTON (33342-331-80) / 80 g in 1 TUBE November 23, 2018
33342-332-15 33342-332 Macleods Pharmaceuticals Limited 1 TUBE in 1 CARTON (33342-332-15) / 15 g in 1 TUBE November 23, 2018
33342-333-15 33342-333 Macleods Pharmaceuticals Limited 1 TUBE in 1 CARTON (33342-333-15) / 15 g in 1 TUBE November 23, 2018
33342-333-54 33342-333 Macleods Pharmaceuticals Limited 454 g in 1 JAR (33342-333-54) November 23, 2018
33342-333-80 33342-333 Macleods Pharmaceuticals Limited 1 TUBE in 1 CARTON (33342-333-80) / 80 g in 1 TUBE November 23, 2018
33342-334-13 33342-334 Macleods Pharmaceuticals Limited 430 g in 1 JAR (33342-334-13) August 18, 2023
16714-267-01 16714-267 NorthStar RxLLC 1 TUBE in 1 CARTON (16714-267-01) / 15 g in 1 TUBE April 21, 2022
16714-267-02 16714-267 NorthStar RxLLC 1 TUBE in 1 CARTON (16714-267-02) / 80 g in 1 TUBE April 21, 2022
16714-267-03 16714-267 NorthStar RxLLC 454 g in 1 JAR (16714-267-03) April 21, 2022
16714-268-01 16714-268 NorthStar RxLLC 1 TUBE in 1 CARTON (16714-268-01) / 15 g in 1 TUBE April 21, 2022
16714-276-01 16714-276 NorthStar RxLLC 1 TUBE in 1 CARTON (16714-276-01) / 15 g in 1 TUBE April 2, 2025
16714-276-02 16714-276 NorthStar RxLLC 1 TUBE in 1 CARTON (16714-276-02) / 80 g in 1 TUBE April 2, 2025
16714-276-03 16714-276 NorthStar RxLLC 454 g in 1 JAR (16714-276-03) April 2, 2025
72603-319-01 72603-319 Northstar Rx LLC 430 g in 1 JAR (72603-319-01) November 1, 2024
68071-1872-8 68071-1872 NuCare Pharmaceuticals,Inc. 80 g in 1 BOX (68071-1872-8) May 4, 2020
68071-2362-5 68071-2362 NuCare Pharmaceuticals,Inc. 1 TUBE in 1 CARTON (68071-2362-5) / 15 g in 1 TUBE March 11, 2021
68071-4286-5 68071-4286 NuCare Pharmaceuticals,Inc. 15 g in 1 BOX (68071-4286-5) February 15, 2018
45802-049-35 45802-049 Padagis Israel Pharmaceuticals Ltd 1 TUBE in 1 CARTON (45802-049-35) / 15 g in 1 TUBE November 10, 2006
45802-054-05 45802-054 Padagis Israel Pharmaceuticals Ltd 454 g in 1 JAR (45802-054-05) July 5, 2007
45802-054-35 45802-054 Padagis Israel Pharmaceuticals Ltd 1 TUBE in 1 CARTON (45802-054-35) / 15 g in 1 TUBE May 12, 2006
45802-054-36 45802-054 Padagis Israel Pharmaceuticals Ltd 1 TUBE in 1 CARTON (45802-054-36) / 80 g in 1 TUBE September 5, 2007
45802-055-05 45802-055 Padagis Israel Pharmaceuticals Ltd 454 g in 1 JAR (45802-055-05) August 4, 2006
45802-055-35 45802-055 Padagis Israel Pharmaceuticals Ltd 1 TUBE in 1 CARTON (45802-055-35) / 15 g in 1 TUBE March 13, 2007
45802-055-36 45802-055 Padagis Israel Pharmaceuticals Ltd 1 TUBE in 1 CARTON (45802-055-36) / 80 g in 1 TUBE October 2, 2006
45802-817-01 45802-817 Padagis Israel Pharmaceuticals Ltd 430 g in 1 JAR (45802-817-01) March 1, 2021
63187-495-15 63187-495 Proficient Rx LP 1 TUBE in 1 CARTON (63187-495-15) / 15 g in 1 TUBE February 2, 2015
71205-033-15 71205-033 Proficient Rx LP 1 TUBE in 1 CARTON (71205-033-15) / 15 g in 1 TUBE May 1, 2018
71205-038-15 71205-038 Proficient Rx LP 1 TUBE in 1 CARTON (71205-038-15) / 15 g in 1 TUBE May 1, 2018
71205-108-15 71205-108 Proficient Rx LP 1 TUBE in 1 CARTON (71205-108-15) / 15 g in 1 TUBE September 4, 2018
71205-108-80 71205-108 Proficient Rx LP 1 TUBE in 1 CARTON (71205-108-80) / 80 g in 1 TUBE September 4, 2018
82804-019-15 82804-019 Proficient Rx LP 1 TUBE in 1 CARTON (82804-019-15) / 15 g in 1 TUBE October 9, 2023
82804-079-30 82804-079 Proficient Rx LP 1 TUBE in 1 CARTON (82804-079-30) / 30 g in 1 TUBE March 13, 2024
70518-3689-0 70518-3689 REMEDYREPACK INC. 1 TUBE in 1 CARTON (70518-3689-0) / 80 g in 1 TUBE March 22, 2023
70518-4205-0 70518-4205 REMEDYREPACK INC. 1 TUBE in 1 CARTON (70518-4205-0) / 15 g in 1 TUBE October 7, 2024
70518-4546-0 70518-4546 REMEDYREPACK INC. 1 TUBE in 1 CARTON (70518-4546-0) / 15 g in 1 TUBE January 15, 2026
67296-2327-1 67296-2327 Redpharm Drug 1 TUBE in 1 CARTON (67296-2327-1) / 15 g in 1 TUBE April 2, 2025
67296-1927-1 67296-1927 RedpharmDrug 1 TUBE in 1 CARTON (67296-1927-1) / 15 g in 1 TUBE September 10, 2015
64380-901-90 64380-901 Strides Pharma Science Limited 430 g in 1 JAR (64380-901-90) June 5, 2020
51672-1284-1 51672-1284 Sun Pharmaceutical Industries, Inc. 1 TUBE in 1 CARTON (51672-1284-1) / 15 g in 1 TUBE September 30, 1994
51672-1284-2 51672-1284 Sun Pharmaceutical Industries, Inc. 1 TUBE in 1 CARTON (51672-1284-2) / 30 g in 1 TUBE October 26, 2016
51672-1284-8 51672-1284 Sun Pharmaceutical Industries, Inc. 1 TUBE in 1 CARTON (51672-1284-8) / 80 g in 1 TUBE September 30, 1994
50090-2244 50090-2244 A-S Medication Solutions — September 30, 1994
50090-3508 50090-3508 A-S Medication Solutions — August 4, 2006
50090-3802 50090-3802 A-S Medication Solutions — September 10, 2015
50090-4761 50090-4761 A-S Medication Solutions — August 4, 2006
50090-5980 50090-5980 A-S Medication Solutions — November 10, 2006
50090-6211 50090-6211 A-S Medication Solutions — July 22, 2016
50090-6978 50090-6978 A-S Medication Solutions — November 23, 2018
50090-7679 50090-7679 A-S Medication Solutions — August 1, 2023
76420-360 76420-360 Asclemed USA, Inc. — February 14, 1978
76420-361 76420-361 Asclemed USA, Inc. — February 14, 1978
63629-8708 63629-8708 Bryant Ranch Prepack — March 1, 2021
63629-8841 63629-8841 Bryant Ranch Prepack — February 14, 1978
72162-1429 72162-1429 Bryant Ranch Prepack — March 1, 2021
72162-2335 72162-2335 Bryant Ranch Prepack — May 12, 2006
72162-2336 72162-2336 Bryant Ranch Prepack — August 4, 2006
46287-010 46287-010 CMP Pharma, Inc. — August 23, 2021
24470-922 24470-922 Cintex Services, LLC — November 10, 2020
0713-0228 0713-0228 Cosette Pharmaceuticals, Inc. — September 10, 2015
0713-0229 0713-0229 Cosette Pharmaceuticals, Inc. — September 10, 2015
61919-619 61919-619 DIRECTRX — February 4, 2021
0168-0005 0168-0005 E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC — February 14, 1978
0168-0006 0168-0006 E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC — February 14, 1978
21922-024 21922-024 Encube Ethicals, Inc. — December 2, 2019
21922-063 21922-063 Encube Ethicals, Inc. — August 1, 2023
68462-797 68462-797 Glenmark Pharmaceuticals Inc., USA — August 22, 2017
68462-798 68462-798 Glenmark Pharmaceuticals Inc., USA — July 22, 2016
33342-331 33342-331 Macleods Pharmaceuticals Limited — November 23, 2018
33342-332 33342-332 Macleods Pharmaceuticals Limited — November 23, 2018
33342-333 33342-333 Macleods Pharmaceuticals Limited — November 23, 2018
33342-334 33342-334 Macleods Pharmaceuticals Limited — August 18, 2023
16714-267 16714-267 NorthStar RxLLC — April 21, 2022
16714-268 16714-268 NorthStar RxLLC — April 21, 2022
16714-276 16714-276 NorthStar RxLLC — April 2, 2025
72603-319 72603-319 Northstar Rx LLC — November 1, 2024
68071-1872 68071-1872 NuCare Pharmaceuticals,Inc. — August 4, 2006
68071-2362 68071-2362 NuCare Pharmaceuticals,Inc. — November 23, 2018
68071-4286 68071-4286 NuCare Pharmaceuticals,Inc. — August 4, 2006
45802-049 45802-049 Padagis Israel Pharmaceuticals Ltd — November 10, 2006
45802-054 45802-054 Padagis Israel Pharmaceuticals Ltd — May 12, 2006
45802-055 45802-055 Padagis Israel Pharmaceuticals Ltd — August 4, 2006
45802-817 45802-817 Padagis Israel Pharmaceuticals Ltd — March 1, 2021
63187-495 63187-495 Proficient Rx LP — November 10, 2006
71205-033 71205-033 Proficient Rx LP — March 3, 2017
71205-038 71205-038 Proficient Rx LP — March 3, 2017
71205-108 71205-108 Proficient Rx LP — August 4, 2006
82804-019 82804-019 Proficient Rx LP — November 23, 2018
82804-079 82804-079 Proficient Rx LP — September 30, 1994
70518-3689 70518-3689 REMEDYREPACK INC. — March 22, 2023
70518-4205 70518-4205 REMEDYREPACK INC. — October 7, 2024
70518-4546 70518-4546 REMEDYREPACK INC. — January 15, 2026
67296-2327 67296-2327 Redpharm Drug — April 2, 2025
67296-1927 67296-1927 RedpharmDrug — September 10, 2015
64380-901 64380-901 Strides Pharma Science Limited — June 5, 2020
51672-1284 51672-1284 Sun Pharmaceutical Industries, Inc. — September 30, 1994

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.