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Serving leading biopharmaceutical companies globally:

Argus Health
Healthtrust
QuintilesIMS
Cipla
Moodys
Cerilliant
Daiichi Sankyo
Chinese Patent Office
Johnson and Johnson
McKinsey

Generated: January 17, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 072629

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NDA 072629 describes ALBUTEROL SULFATE, which is a drug marketed by Actavis Mid Atlantic, Apotex Inc, Aurobindo Pharma Ltd, Bausch And Lomb, Copley Pharm, Hi Tech Pharma, Landela Pharm, Mylan Speclt, Nephron, Ritedose Corp, Roxane, Sun Pharma Global, Teva Pharms, Watson Labs, Watson Labs Inc, Wockhardt Eu Operatn, Amneal Pharms, G And W Labs Inc, Mova, Teva, Vintage, Vistapharm, Mylan, Am Therap, Dava Pharms Inc, Pliva, Sandoz, Sun Pharm Industries, Ucb Inc, Warner Chilcott, Cipla Ltd, Sandoz Inc, and Watson Labs Teva, and is included in sixty-six NDAs. It is available from thirty-five 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. Seventeen suppliers are listed for this compound. Additional details are available on the albuterol sulfate; ipratropium bromide profile page.
Summary for 072629
Tradename:ALBUTEROL SULFATE
Applicant:Watson Labs
Ingredient:albuterol sulfate
Patents:0
Therapeutic Class:Respiratory Tract Agents
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrengthEQ 2MG BASE
Approval Date:Jan 31, 1991TE:RLD:No

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Serving leading biopharmaceutical companies globally:

Chinese Patent Office
US Department of Justice
Federal Trade Commission
Deloitte
Cantor Fitzgerald
McKesson
Chubb
Moodys
Harvard Business School

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