Active Ingredient: CIMETIDINE HYDROCHLORIDE
Proprietary Name: TAGAMET
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 300MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017924
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: GLAXOSMITHKLINE
Marketing Status:
Discontinued
Patent and Exclusivity Information
