Active Ingredient: RANITIDINE HYDROCHLORIDE
Proprietary Name: ZANTAC
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 25MG BASE/ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019090
Product Number: 001
Approval Date: Oct 19, 1984
Applicant Holder Full Name: PAI HOLDINGS LLC DBA PHARMACEUTICAL ASSOCIATES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information