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: A074541
Product Number: 001
Approval Date: Aug 5, 1997
Applicant Holder Full Name: CYCLE PHARMACEUTICALS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information
