FDA Approves Unique Low Dosage of Zubsolv®
Uppsala, Sweden – October 6, 2016 – Orexo AB (publ.) announced today that 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. The new dosage is expected to be available in US pharmacies in early 2017. This new introduction extends Orexo’s best-in-class offering of the broadest dosage ranges of any buprenorphine/naloxone product on the US market to six individual dosage strengths. By offering the broadest dosage range,