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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: Application Number: A205106
Product Number: 001
Approval Date: Sep 21, 2018
Applicant Holder Full Name: ARTHUR GROUP LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information