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Abbreviated New Drug Application (ANDA): 075696
Company: ACTAVIS ELIZABETH
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ETODOLAC ETODOLAC 400MG TABLET, EXTENDED RELEASE;ORAL Discontinued None No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
07/31/2000 ORIG-1 Approval Letter (PDF)

Label is not available on this site.

https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2000/75696ltr.pdf
Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
04/28/2021 SUPPL-16 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

05/09/2016 SUPPL-15 Labeling-Package Insert

Label is not available on this site.

02/05/2016 SUPPL-14 Labeling-Package Insert

Label is not available on this site.

09/23/2004 SUPPL-10 Labeling

Label is not available on this site.

11/02/2001 SUPPL-4 Manufacturing (CMC)-Control

Label is not available on this site.

10/05/2001 SUPPL-2 Manufacturing (CMC)-Facility

Label is not available on this site.

05/07/2001 SUPPL-1 Manufacturing (CMC)-Control

Label is not available on this site.

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