Targiniq Approved for Long-Term Pain Management
July 23, 2014 - The U.S. Food and Drug Administration (FDA) approved Targiniq ER (oxycodone/naloxone) manufacturerd by Purdue Pharma. Targiniq is a controlled-release, fixed-dose formulation of oxycodone and naloxone that is to be administered every 12 hours for the management of severe pain severe that requires continuous opioid treatment and for which alternative treatment options are inadequate.
Targiniq ER will be available in three dosage strengths (oxycodone/naloxone): 10mg/5mg, 20mg/10mg, and 40mg/20mg extended-release tablets. Launch information is not yet available.
Adverse reactions or quality problems experienced with the use of a recalled product may be reported to the FDA’s MedWatch Adverse Event Reporting Program either online, by regular mail or by fax.
- Complete and submit the report Online: www.fda.gov/medwatch/report.htm
- Regular Mail or Fax: Download form www.fda.gov/MedWatch/getforms.htm or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178
Actual drug patent expiration dates and availability of new medications are subject to change due to patent litigation, settlement agreements, additional patents, exclusivities, and final FDA approval. Distribution and availability of new medications at pharmacies may not occur immediately following FDA approval. Patients are advised to speak with their healthcare professional or pharmacist regarding appropriateness as well as actual availability.
*This is provided for information only. The reference to any medication above does not mean the medication is covered by your plan.