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: A074023
Product Number: 001
Approval Date: Aug 22, 1997
Applicant Holder Full Name: MYLAN PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information