05.10.2017 13:15:11
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Neurocrine Announces FDA Approval Of 80 Mg Capsule Of INGREZZA - Quick Facts
(RTTNews) - Neurocrine Biosciences, Inc. (NBIX) announced the U.S. FDA has approved an 80 mg INGREZZA (valbenazine) capsule strength to be used for the treatment of adults with tardive dyskinesia. The 80 mg capsule of INGREZZA will be available for patients within two weeks through a select pharmacy network.
INGREZZA, a selective vesicular monoamine transporter 2 (VMAT2) inhibitor, which was approved by the FDA April 11, 2017, is the first FDA-approved product indicated for the treatment of adults with tardive dyskinesia.

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