Active Ingredient: FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 60MG;120MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076236
Product Number: 001
Approval Date: Apr 14, 2005
Applicant Holder Full Name: BARR LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
