Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 075696
Company: ACTAVIS ELIZABETH
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. |
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09/23/2004 | SUPPL-10 | Labeling |
Label is not available on this site. |
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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. |