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Last Updated: March 29, 2024

Details for New Drug Application (NDA): 084319


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NDA 084319 describes TRIAMCINOLONE, which is a drug marketed by Barr, Impax Labs, Ivax Sub Teva Pharms, Mylan, Purepac Pharm, Roxane, Sandoz, Teva, Watson Labs, Actavis Mid Atlantic, Alkem Labs Ltd, Alpharma Us Pharms, Ambix, Chartwell Rx, Cosette, Encube, Fougera Pharms, Glenmark Pharms Ltd, Macleods Pharms Ltd, Micro Labs, Morton Grove, Padagis Us, Pharmaderm, Pharmafair, Strides Pharma, Taro, Topiderm, Amneal, Eugia Pharma, Long Grove Pharms, Mylan Labs Ltd, Parnell, Teva Pharms Usa, Epic Pharma Llc, Pai Holdings Pharm, Quagen, Wockhardt Bio Ag, Aurobindo Pharma Ltd, Cintex Svcs, Glenmark Pharms, Padagis Israel, Akorn, Lyne, Apotex, Perrigo Pharma Intl, and Rising, and is included in one hundred and fourteen NDAs. Additional details are available on the TRIAMCINOLONE profile page.

The generic ingredient in TRIAMCINOLONE is triamcinolone diacetate. There are fifty-one drug master file entries for this compound. Additional details are available on the triamcinolone diacetate profile page.
Summary for 084319
Tradename:TRIAMCINOLONE
Applicant:Barr
Ingredient:triamcinolone
Patents:0
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 084319

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength4MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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