Zalicus Announces FDA Approval of 32mg Dose Strength of EXALGO®
Provides additional dosage options to help control chronic pain in opioid-tolerant patients
Zalicus receives royalties on EXALGO sales
Zalicus Inc. (ZLCS), a biopharmaceutical company that discovers and develops novel treatments for patients suffering from pain and immuno-inflammatory diseases, today announced that the U.S. Food and Drug Administration (FDA) has approved the supplemental new drug application (sNDA) filed by Mallinckrodt Inc., a subsidiary of Covidien plc, for the 32 mg dose strength of EXALGO® (hydromorphone HCl) Extended-Release Tablets (CII), for the management of moderate to severe pain in opioid-tolerant patients requiring continuous, around-the-clock opioid analgesia for an extended period of time.
- Published: 27 August 2012
- Written by Editor