Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 074110
Company: HAMILTON PHARMS
Company: HAMILTON PHARMS
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| NAPROXEN | NAPROXEN | 250MG | TABLET;ORAL | Discontinued | None | No | No |
| NAPROXEN | NAPROXEN | 375MG | TABLET;ORAL | Discontinued | None | No | No |
| NAPROXEN | NAPROXEN | 500MG | 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 |
|---|---|---|---|---|---|---|---|
| 10/30/1992 | 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 |
|---|---|---|---|---|---|
| 12/28/1995 | SUPPL-5 | Labeling |
Label is not available on this site. |
||
| 02/17/1995 | SUPPL-2 | Labeling |
Label is not available on this site. |