Generated: September 23, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 077788
describes ALBUTEROL SULFATE
, which is a drug marketed by Mova, Vintage, Copley Pharm, Pliva, Apotex Inc, Warner Chilcott, Teva, Ucb Inc, Roxane, Watson Labs, Actavis Mid Atlantic, Sun Pharm Inds, Ritedose Corp, Amneal Pharms, Hi Tech Pharma, Teva Pharms, Am Therap, Bausch And Lomb, Sandoz, Mylan Speclt, G And W Labs Inc, Nephron, Sun Pharma Global, Dava Pharms Inc, Landela Pharm, Watson Labs Inc, Vistapharm, Mylan, Wockhardt Eu Operatn, Cipla Ltd, Watson Labs Teva, and Sandoz Inc, and is included in sixty-five NDAs. It is available from thirty-one suppliers. Additional details are available on the ALBUTEROL SULFATE profile page.
The generic ingredient in ALBUTEROL SULFATE is albuterol sulfate; ipratropium bromide. There are thirty-seven drug master file entries for this compound. Fourteen suppliers are listed for this compound. Additional details are available on the albuterol sulfate; ipratropium bromide profile page.
Suppliers and Packaging for NDA: 077788
||National Drug Code
||NDA AUTHORIZED GENERIC
||12 BOTTLE in 1 CASE (66689-100-08) > 473 mL in 1 BOTTLE (66689-100-16)
|Complete Access Available with Subscription
Summary for product number 001
|Active Rx/OTC/Discontinued:||RX||Dosage:||SYRUP;ORAL||Strength||EQ 2MG BASE/5ML|
|Approval Date:||Jun 26, 2007||TE:||AA||RLD:||No|
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