Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 016942
Company: WESTWOOD SQUIBB
Company: WESTWOOD SQUIBB
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| HALOTEX | HALOPROGIN | 1% | CREAM;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 1 - New Molecular Entity | 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 |
|---|---|---|---|---|---|
| 05/28/1986 | SUPPL-17 | Labeling |
Label is not available on this site. |
||
| 04/26/1996 | SUPPL-14 | Labeling |
Label is not available on this site. |
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| 04/26/1996 | SUPPL-13 | Labeling |
Label is not available on this site. |
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| 12/22/1977 | SUPPL-11 | Labeling |
Label is not available on this site. |