Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: RANITIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: SYRUP; ORAL
Strength: EQ 15MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A077405
Product Number: 001
Approval Date: Sep 21, 2007
Applicant Holder Full Name: PHARMACEUTICAL ASSOCIATES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
