Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 076906
Company: APOTEX
Company: APOTEX
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| FOSINOPRIL SODIUM | FOSINOPRIL SODIUM | 10MG | TABLET;ORAL | Discontinued | None | No | No |
| FOSINOPRIL SODIUM | FOSINOPRIL SODIUM | 20MG | TABLET;ORAL | Discontinued | None | No | No |
| FOSINOPRIL SODIUM | FOSINOPRIL SODIUM | 40MG | 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 |
|---|---|---|---|---|---|---|---|
| 05/17/2005 | 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 |
|---|---|---|---|---|---|
| 12/31/2013 | SUPPL-10 | Labeling-Package Insert |
Label is not available on this site. |
||
| 04/08/2011 | SUPPL-9 | Labeling-Package Insert |
Label is not available on this site. |
||
| 10/28/2010 | SUPPL-8 | Labeling-Package Insert |
Label is not available on this site. |