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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 217159

APHEXDA (MOTIXAFORTIDE ACETATE)
EQ 62MG BASE/VIAL
Marketing Status: Prescription
Active Ingredient: MOTIXAFORTIDE ACETATE
Proprietary Name: APHEXDA
Dosage Form; Route of Administration: POWDER; SUBCUTANEOUS
Strength: EQ 62MG BASE/VIAL
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N217159
Product Number: 001
Approval Date: Sep 8, 2023
Applicant Holder Full Name: BIOLINERX LTD
Marketing Status:  Prescription
Patent and Exclusivity Information
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