Active Ingredient: CIMETIDINE HYDROCHLORIDE
Proprietary Name: CIMETIDINE HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: EQ 6MG BASE/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074269
Product Number: 001
Approval Date: Dec 27, 1994
Applicant Holder Full Name: HOSPIRA WORLDWIDE, INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
