Last Updated: November 13, 2026

Details for New Drug Application (NDA): 206379

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NDA 206379 describes TRIAMCINOLONE ACETONIDE, which is a drug marketed by Actavis Mid Atlantic, Alkem Labs Ltd, Alpharma Us Pharms, Ambix, Chartwell Rx, Cosette Pharms Nc, Encube, Fougera Pharms, Glenmark Pharms Ltd, Macleods Pharms, Micro Labs, Morton Grove, Padagis Us, Pharmaderm, Pharmafair, Pharmobedient, Strides Pharma, Sun Pharma Canada, Taro, Topiderm, Alembic, Amneal, Caplin, Dr Reddys, Eugia Pharma, Hikma, Long Grove Pharms, Mylan Labs Ltd, Parnell, Sandoz, Teva Pharms Usa, Watson Labs, Beach Prods, Epic Pharma Llc, Quagen, Aurobindo Pharma Ltd, Extrovis, Glenmark Speclt, Padagis Israel, Pharmazone, Rising, Sciegen Pharms, Apotex, and Perrigo Pharma Intl, and is included in ninety-eight NDAs. It is available from seventy suppliers. Additional details are available on the TRIAMCINOLONE ACETONIDE profile page.

The generic ingredient in TRIAMCINOLONE ACETONIDE is triamcinolone acetonide. There is one drug master file entry for this compound. Eighty suppliers are listed for this compound. Additional details are available on the triamcinolone acetonide profile page.

Summary for 206379

Tradename:	TRIAMCINOLONE ACETONIDE
Applicant:	Glenmark Pharms Ltd
Ingredient:	triamcinolone acetonide
Patents:	0

Pharmacology for NDA: 206379

Mechanism of Action	Corticosteroid Hormone Receptor Agonists

Medical Subject Heading (MeSH) Categories for 206379

Anti-Inflammatory Agents
Glucocorticoids
Immunosuppressive Agents

Suppliers and Packaging for NDA: 206379

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
TRIAMCINOLONE ACETONIDE	triamcinolone acetonide	OINTMENT;TOPICAL	206379	ANDA	A-S Medication Solutions	50090-6211	50090-6211-0	1 TUBE in 1 CARTON (50090-6211-0) / 15 g in 1 TUBE
TRIAMCINOLONE ACETONIDE	triamcinolone acetonide	OINTMENT;TOPICAL	206379	ANDA	Glenmark Pharmaceuticals Inc., USA	68462-798	68462-798-17	1 TUBE in 1 CARTON (68462-798-17) / 15 g in 1 TUBE

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	OINTMENT;TOPICAL			Strength	0.5%
Approval Date:	Jul 22, 2016	TE:		RLD:	No

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