Active Ingredient: BUSULFAN
Proprietary Name: BUSULFEX
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 6MG/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N020954
Product Number: 001
Approval Date: Feb 4, 1999
Applicant Holder Full Name: OTSUKA PHARMACEUTICAL CO LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
