Viibryd Approved in a New Strength
March 6, 2015 – The U.S. Food and Drug Administration (FDA) approved Viibryd (vilazodone), manufactured by Actavis, for a new strength of 20mg. Viibryd is both a selective serotonin reuptake inhibitor (SSRI) and a 5-HT1A receptor partial agonist indicated to treat adults with major depressive disorder. Viibryd was previously available in 10mg and 40mg tablets and is taken once a day. The 20mg tablets were launched immediately after approval.
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 a 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.