Issued to Actavis, L.L.C.. Application reviewed but not approved; deficiencies must be corrected.
Issued
September 26, 2017Application
NDA 505b1 • 208419
Product
PEMETREXED
Company
Actavis, L.L.C.
Review center
Other
Stage
Final Decision
Response due
January 1, 2022
Assyro regulatory brief
FreeSource facts and Assyro context are separated so you can scan the action quickly without treating analysis as an FDA conclusion.
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.
Open the document workspaceFDA source document
Application reviewed but not approved; deficiencies must be corrected. Requires resubmission addressing deficiencies. FDA issued this letter to Actavis, L.L.C. on September 26, 2017.
NDA 208419 is the application under which FDA issued this complete response letter for PEMETREXED to Actavis, L.L.C.. It was reviewed by FDA Other. The letter is dated September 26, 2017.
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.