Active Ingredient: EFLORNITHINE HYDROCHLORIDE
Proprietary Name: ORNIDYL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 200MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019879
Product Number: 002
Approval Date: Nov 28, 1990
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
