Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: ZANTAC
Dosage Form; Route of Administration: SYRUP; ORAL
Strength: EQ 15MG BASE/ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019675
Product Number: 001
Approval Date: Dec 30, 1988
Applicant Holder Full Name: GLAXO GROUP LTD ENGLAND DBA GLAXOSMITHKLINE
Marketing Status:
Discontinued
Patent and Exclusivity Information