Active Ingredient: FEXOFENADINE HYDROCHLORIDE
Proprietary Name: FEXOFENADINE HYDROCHLORIDE
Dosage Form; Route of Administration: SUSPENSION; ORAL
Strength: 30MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A201311
Product Number: 001
Approval Date: Jul 25, 2012
Applicant Holder Full Name: P AND L DEVELOPMENT LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information