Active Ingredient: FAMOTIDINE
Proprietary Name: FAMOTIDINE PRESERVATIVE FREE IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.4MG/ML
Reference Listed Drug: No
Reference Standard: Yes
TE Code:
Application Number: A075591
Product Number: 001
Approval Date: May 10, 2001
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:
Prescription
Patent and Exclusivity Information
