Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 075844
Company: SUN PHARM INDS INC
Company: SUN PHARM INDS INC
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| OXAPROZIN | OXAPROZIN | 600MG | TABLET;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 |
|---|---|---|---|---|---|---|---|
| 01/03/2002 | ORIG-1 | Approval |
Label is not available on this site. |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 08/09/2007 | SUPPL-11 | Labeling |
Label is not available on this site. |
||
| 06/19/2007 | SUPPL-10 | Labeling |
Label is not available on this site. |
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| 06/08/2006 | SUPPL-9 | Labeling |
Label is not available on this site. |
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| 02/07/2006 | SUPPL-8 | Labeling |
Label is not available on this site. |
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| 03/21/2003 | SUPPL-6 | Labeling |
Label is not available on this site. |
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| 06/12/2002 | SUPPL-1 | Manufacturing (CMC)-Control |
Label is not available on this site. |