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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 210296

BAFIERTAM (MONOMETHYL FUMARATE)
95MG
Marketing Status: Prescription
Active Ingredient: MONOMETHYL FUMARATE
Proprietary Name: BAFIERTAM
Dosage Form; Route of Administration: CAPSULE, DELAYED RELEASE; ORAL
Strength: 95MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N210296
Product Number: 001
Approval Date: Apr 28, 2020
Applicant Holder Full Name: BANNER LIFE SCIENCES LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
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