Generated: November 20, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 062835
, which is a drug marketed by Watson Labs, Teva, Mayne Pharma Inc, Quantum Pharmics, Wockhardt, Paddock Llc, G And W Labs Inc, Vintage, Odyssey Pharms, Fougera Pharms Inc, Pharmaderm, Nesher Pharms, Pharm Assoc, Taro, Vistapharm, Fougera Pharms, Usl Pharma, Perrigo New York, Allied Pharma Inc, Crown Labs Inc, Morton Grove, Gavis Pharms, Lyne, Sun Pharm Inds, Actavis Mid Atlantic, Pharmafair, Hi Tech Pharma, Vintage Pharms, Fougera, Sandoz, Alpharma Us Pharms, Heritage Pharms Inc, X Gen Pharms, Taro Pharm, Upsher-smith Labs, Glenmark Pharms Ltd, Akorn, Dr Reddys Labs Ltd, Perrigo Uk Finco, Riconpharma Llc, and Teligent Pharma Inc, and is included in seventy-one NDAs. It is available from forty-nine suppliers. Additional details are available on the NYSTATIN profile page.
The generic ingredient in NYSTATIN is nystatin; triamcinolone acetonide. There are eight drug master file entries for this compound. Eighteen suppliers are listed for this compound. Additional details are available on the nystatin; triamcinolone acetonide profile page.
Summary for 062835
|Formulation / Manufacturing:||see details|Complete Access Available with Subscription
Summary for product number 001
|Active Rx/OTC/Discontinued:||DISCN||Dosage:||SUSPENSION;ORAL||Strength||100,000 UNITS/ML|
|Approval Date:||Nov 19, 1987||TE:||RLD:||No|
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