Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: RANITIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 150MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075165
Product Number: 001
Approval Date: Sep 30, 1998
Applicant Holder Full Name: HERITAGE PHARMA LABS INC DBA AVET PHARMACEUTICALS LABS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information