Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 016943
Company: WESTWOOD SQUIBB
Company: WESTWOOD SQUIBB
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| HALOTEX | HALOPROGIN | 1% | SOLUTION;TOPICAL | 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 |
|---|---|---|---|---|---|---|---|
| 08/06/1971 | ORIG-1 | Approval | Type 3 - New Dosage Form | PRIORITY |
Label is not available on this site. |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 01/26/1990 | SUPPL-10 | Labeling |
Label is not available on this site. |
||
| 01/09/1997 | SUPPL-9 | Labeling |
Label is not available on this site. |