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Active Ingredient: BORTEZOMIB
Proprietary Name: BORTEZOMIB
Dosage Form; Route of Administration: POWDER; INTRAVENOUS
Strength: 3.5MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: Application Number: N205004
Product Number: 001
Approval Date: Nov 6, 2017
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
