DURECT Announces FDA Acceptance of REMOXY® NDA, PDUFA Date of September 25, 2016
CUPERTINO, Calif., April 12, 2016 /PRNewswire/ — DURECT Corporation (Nasdaq: DRRX) today announced its licensee, Pain Therapeutics (Nasdaq: PTIE), has been informed by the U.S. Food and Drug Administration (FDA) that the New Drug Application (NDA) for REMOXY®, an abuse-deterrent formulation of extended-release oxycodone (CII) capsules, is sufficiently complete to permit a substantive review, and that […]
DURECT Announces FDA Acceptance of REMOXY® NDA, PDUFA Date of September 25, 2016 Read More »