Thursday, July 12, 2018

NDA for ADHD Med That Is Dosed at Night Resubmitted to FDA - Monthly Prescribing Reference


NDA for ADHD Med That Is Dosed at Night Resubmitted to FDA
Monthly Prescribing Reference
The Food and Drug Administration (FDA) has accepted a resubmitted New Drug Application (NDA) for the investigational treatment HLD200 (Ironshore Pharmaceuticals) for attention deficit hyperactivity disorder (ADHD). HLD200, a delayed-release and ...
Ironshore Pharmaceuticals Announces PDUFA Date of August 8, 2018 for HLD200Odessa American

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