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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 208392

BORTEZOMIB (BORTEZOMIB)
3.5MG/VIAL
Marketing Status: Prescription
Active Ingredient: BORTEZOMIB
Proprietary Name: BORTEZOMIB
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS, SUBCUTANEOUS
Strength: 3.5MG/VIAL
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A208392
Product Number: 001
Approval Date: May 2, 2022
Applicant Holder Full Name: PHARMASCIENCE INC
Marketing Status:  Prescription
Patent and Exclusivity Information
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