Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 089959
Company: SANDOZ
Company: SANDOZ
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| PROPOXYPHENE HYDROCHLORIDE AND ACETAMINOPHEN | ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE | 650MG;65MG | 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 |
|---|---|---|---|---|---|---|---|
| 07/18/1989 | 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 |
|---|---|---|---|---|---|
| 01/08/2001 | SUPPL-8 | Manufacturing (CMC)-Control |
Label is not available on this site. |
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| 09/25/1996 | SUPPL-7 | Manufacturing (CMC) |
Label is not available on this site. |
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| 05/11/1998 | SUPPL-6 | Manufacturing (CMC) |
Label is not available on this site. |
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| 06/28/1993 | SUPPL-5 | Labeling |
Label is not available on this site. |
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| 05/17/1991 | SUPPL-4 | Labeling |
Label is not available on this site. |
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| 04/07/1992 | SUPPL-3 | Manufacturing (CMC) |
Label is not available on this site. |
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| 08/22/1990 | SUPPL-2 | Manufacturing (CMC) |
Label is not available on this site. |
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| 10/26/1989 | SUPPL-1 | Labeling |
Label is not available on this site. |