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Generated: December 18, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 205782

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NDA 205782 describes TRIAMCINOLONE ACETONIDE, which is a drug marketed by Actavis Mid Atlantic, Alpharma Us Pharms, Ambix, Fougera Pharms, G And W Labs, Glenmark Pharms Ltd, Lupin Atlantis, Morton Grove, Mylan Pharms Inc, Perrigo New York, Pharmaderm, Pharmafair, Taro, Teligent Pharma Inc, Topiderm, Vintage, Parnell, Sandoz Inc, Watson Labs, Akorn, G And W Labs Inc, Wockhardt, Wockhardt Eu Operatn, Glenmark Pharms, Lyne, Perrigo Israel, Perrigo Uk Finco, Riconpharma Llc, and Cmp Pharma Inc, and is included in seventy-seven NDAs. It is available from sixty-two suppliers. Additional details are available on the TRIAMCINOLONE ACETONIDE profile page.

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

Summary for 205782

Pharmacology for NDA: 205782

Medical Subject Heading (MeSH) Categories for 205782

Suppliers and Packaging for NDA: 205782

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
TRIAMCINOLONE ACETONIDE triamcinolone acetonide SPRAY;TOPICAL 205782 ANDA Perrigo New York Inc 45802-045 45802-045-01 63 g in 1 CAN (45802-045-01)
TRIAMCINOLONE ACETONIDE triamcinolone acetonide SPRAY;TOPICAL 205782 ANDA Perrigo New York Inc 45802-045 45802-045-02 100 g in 1 CAN (45802-045-02)

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:SPRAY;TOPICALStrength0.147MG/GM
Approval Date:Apr 13, 2015TE:ATRLD:No


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US Department of Justice
McKinsey

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