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Serving hundreds of leading biopharmaceutical companies globally:

Fish and Richardson
Teva
McKesson
US Department of Justice
AstraZeneca
Cipla
QuintilesIMS
Johnson and Johnson
Argus Health

Generated: April 20, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 201311

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NDA 201311 describes FEXOFENADINE HYDROCHLORIDE, which is a drug marketed by Barr, Actavis Mid Atlantic, Dr Reddys Labs Ltd, Mylan, Teva, Aurolife Pharma Llc, Hetero Labs Ltd V, Sciegen Pharms Inc, Sun Pharm Inds, Wockhardt Ltd, Aurobindo Pharma Ltd, Impax Pharms, and Sun Pharma Global, and is included in seventeen NDAs. It is available from sixty-seven suppliers. Additional details are available on the FEXOFENADINE HYDROCHLORIDE profile page.

The generic ingredient in FEXOFENADINE HYDROCHLORIDE is fexofenadine hydrochloride; pseudoephedrine hydrochloride. There are twenty-three drug master file entries for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the fexofenadine hydrochloride; pseudoephedrine hydrochloride profile page.
Summary for 201311
Tradename:FEXOFENADINE HYDROCHLORIDE
Applicant:Actavis Mid Atlantic
Ingredient:fexofenadine hydrochloride
Patents:0
Therapeutic Class:Respiratory Tract Agents
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:SUSPENSION;ORALStrength30MG/5ML
Approval Date:Jul 25, 2012TE:ABRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Teva
Cerilliant
Cantor Fitzgerald
Express Scripts
Fish and Richardson
US Army
Colorcon
US Department of Justice
Harvard Business School

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