U.S. flag An official website of the United States government
  1. Home
  2. Drug Databases
  3. Orange Book Home

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 019675

ZANTAC (RANITIDINE HYDROCHLORIDE)
EQ 15MG BASE/ML
Marketing Status: Discontinued
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
Back to Top