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VUMERITY (Biogen Australia Pty Ltd)

Product name
VUMERITY
Date registered
Evaluation commenced
Decision date
Approval time
197 (255 working days)
Active ingredients
diroximel fumarate
Registration type
NCE/NBE
Indication

VUMERITY (enteric capsule) is indicated in patients with relapsing multiple sclerosis to reduce the frequency of relapses and to delay the progression of disability.

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