Issued to Cadence Pharmaceuticals. Application reviewed but not approved; deficiencies must be corrected.
Issued
February 10, 2010Application
NDA 505b1 • 022450
Product
OFIRMEV
Company
Cadence Pharmaceuticals
Review center
Other
Stage
Final Decision
Response due
November 13, 2026
Assyro regulatory brief
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FDA's complete response letter contains source-text evidence related to Labeling, packaging, and proprietary name, Facility inspection and CGMP compliance. Theme counts identify where the letter discusses a topic; they do not replace review of the exact redacted letter.
Review the exact redacted FDA letter and address each stated deficiency before resubmission.
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Application reviewed but not approved; deficiencies must be corrected. Requires resubmission addressing deficiencies. FDA issued this letter to Cadence Pharmaceuticals on February 10, 2010.
NDA 022450 is the application under which FDA issued this complete response letter for OFIRMEV to Cadence Pharmaceuticals. It was reviewed by FDA Other. The letter is dated February 10, 2010.
FDA will not approve the application in its present form. The sponsor can resubmit after addressing every deficiency listed in the letter — which starts a Class 1 (two-month) or Class 2 (six-month) resubmission review clock — withdraw the application, or request an opportunity for a hearing.