Last Updated: November 8, 2026

Details for New Drug Application (NDA): 208763

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NDA 208763 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 208763

Tradename:	TRIAMCINOLONE ACETONIDE
Applicant:	Chartwell Rx
Ingredient:	triamcinolone acetonide
Patents:	0

Medical Subject Heading (MeSH) Categories for 208763

Anti-Inflammatory Agents
Glucocorticoids
Immunosuppressive Agents

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	CREAM;TOPICAL			Strength	0.025%
Approval Date:	Feb 1, 2017	TE:	AT	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	CREAM;TOPICAL			Strength	0.1%
Approval Date:	Feb 1, 2017	TE:	AT	RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	RX	Dosage:	CREAM;TOPICAL			Strength	0.5%
Approval Date:	Feb 1, 2017	TE:	AT	RLD:	No

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