Active Ingredient: CIMETIDINE HYDROCHLORIDE
Proprietary Name: CIMETIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 300MG BASE/2ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074005
Product Number: 001
Approval Date: Aug 31, 1994
Applicant Holder Full Name: VINTAGE PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
