Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 202978

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CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY (FEXOFENADINE HYDROCHLORIDE)
30MG
Marketing Status: Discontinued

Active Ingredient: FEXOFENADINE HYDROCHLORIDE
Proprietary Name: CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY
Dosage Form; Route of Administration: TABLET, ORALLY DISINTEGRATING; ORAL
Strength: 30MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A202978
Product Number: 001
Approval Date: Jan 18, 2013
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:  Discontinued
Patent and Exclusivity Information

CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES (FEXOFENADINE HYDROCHLORIDE)
30MG
Marketing Status: Discontinued

Active Ingredient: FEXOFENADINE HYDROCHLORIDE
Proprietary Name: CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES
Dosage Form; Route of Administration: TABLET, ORALLY DISINTEGRATING; ORAL
Strength: 30MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A202978
Product Number: 002
Approval Date: Jan 18, 2013
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:  Discontinued
Patent and Exclusivity Information