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: A207794
Product Number: 001
Approval Date: Jan 14, 2019
Applicant Holder Full Name: NEXUS PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information