Active Ingredient: BUSULFAN
Proprietary Name: BUSULFAN
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 6MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A205139
Product Number: 001
Approval Date: Dec 8, 2017
Applicant Holder Full Name: ACTAVIS LLC AN INDIRECT WHOLLY OWNED SUB OF TEVA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information