Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: RANITIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 75MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075294
Product Number: 001
Approval Date: Mar 28, 2000
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:
Over-the-counter
Patent and Exclusivity Information