Active Ingredient: FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 180MG;240MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A215232
Product Number: 001
Approval Date: Apr 17, 2025
Applicant Holder Full Name: AUROBINDO PHARMA LTD
Marketing Status:
Over-the-counter
Patent and Exclusivity Information
