Active Ingredient: CIMETIDINE HYDROCHLORIDE
Proprietary Name: TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 6MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019434
Product Number: 001
Approval Date: Oct 31, 1985
Applicant Holder Full Name: GLAXOSMITHKLINE
Marketing Status:
Discontinued
Patent and Exclusivity Information
