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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: AP
Application Number: A210448
Product Number: 001
Approval Date: May 7, 2019
Applicant Holder Full Name: APOTEX INC
Marketing Status:
Prescription
Patent and Exclusivity Information