Active Ingredient: DIROXIMEL FUMARATE
Proprietary Name: VUMERITY
Dosage Form; Route of Administration: CAPSULE, DELAYED RELEASE; ORAL
Strength: 231MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N211855
Product Number: 001
Approval Date: Oct 29, 2019
Applicant Holder Full Name: BIOGEN INC
Marketing Status:
Prescription
Patent and Exclusivity Information
