Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 076191

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FEXOFENADINE HYDROCHLORIDE (FEXOFENADINE HYDROCHLORIDE)
30MG
Marketing Status: Discontinued

Active Ingredient: FEXOFENADINE HYDROCHLORIDE
Proprietary Name: FEXOFENADINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 30MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076191
Product Number: 001
Approval Date: Aug 31, 2005
Applicant Holder Full Name: BARR LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

FEXOFENADINE HYDROCHLORIDE (FEXOFENADINE HYDROCHLORIDE)
60MG
Marketing Status: Discontinued

Active Ingredient: FEXOFENADINE HYDROCHLORIDE
Proprietary Name: FEXOFENADINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 60MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076191
Product Number: 002
Approval Date: Aug 31, 2005
Applicant Holder Full Name: BARR LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

FEXOFENADINE HYDROCHLORIDE (FEXOFENADINE HYDROCHLORIDE)
180MG
Marketing Status: Discontinued

Active Ingredient: FEXOFENADINE HYDROCHLORIDE
Proprietary Name: FEXOFENADINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 180MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A076191
Product Number: 003
Approval Date: Aug 31, 2005
Applicant Holder Full Name: BARR LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information