Active Ingredient: CIMETIDINE HYDROCHLORIDE
Proprietary Name: CIMETIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 300MG BASE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074553
Product Number: 001
Approval Date: Jan 27, 1997
Applicant Holder Full Name: PHARMACEUTICAL ASSOCIATES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information