Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 074432
Company: PLIVA
Company: PLIVA
Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
---|---|---|---|---|---|---|---|
DICLOFENAC SODIUM | DICLOFENAC SODIUM | 50MG | TABLET, DELAYED RELEASE;ORAL | Discontinued | None | No | No |
DICLOFENAC SODIUM | DICLOFENAC SODIUM | 75MG | TABLET, DELAYED 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 |
---|---|---|---|---|---|---|---|
07/29/1999 | ORIG-1 | Approval |
Letter (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/1999/74432ltr.pdf |
Supplements
Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
---|---|---|---|---|---|
05/09/2016 | SUPPL-17 | Labeling-Package Insert |
Label is not available on this site. |
||
01/08/2007 | SUPPL-13 | Labeling |
Label is not available on this site. |
||
02/23/2006 | SUPPL-9 | Labeling |
Label is not available on this site. |
||
03/25/2002 | SUPPL-3 | Labeling |
Label is not available on this site. |
||
06/29/2001 | SUPPL-2 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
07/07/2000 | SUPPL-1 | Manufacturing (CMC)-Facility |
Label is not available on this site. |