October 6, 2016 / 6:11 AM / a year ago

BRIEF-Orexo says receives FDA approval for Zubsolv

Oct 6 (Reuters) - Orexo AB

* Says it has received approval from the US Food and Drug Administration (FDA) of a new unique low dose, 0.7mg/0.18 mg, tablet of Zubsolv (buprenorphine/naloxone) sublingual tablet (CIII) for the treatment of opioid dependence

* Says the new dosage is expected to be available in US pharmacies in early 2017 Source text for Eikon: Further company coverage: (Stockholm Newsroom)

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