Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 074613
Company: TEVA PARENTERAL
Company: TEVA PARENTERAL
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| BUMETANIDE | BUMETANIDE | 0.25MG/ML | INJECTABLE;INJECTION | 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 |
|---|---|---|---|---|---|---|---|
| 11/18/1997 | 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 |
|---|---|---|---|---|---|
| 08/09/2000 | SUPPL-3 | Labeling |
Label is not available on this site. |
||
| 05/18/1999 | SUPPL-2 | Labeling |
Label is not available on this site. |
||
| 09/20/1999 | SUPPL-1 | Manufacturing (CMC) |
Label is not available on this site. |