Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 016998
Company: PARKE DAVIS
Company: PARKE DAVIS
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| UTICORT | BETAMETHASONE BENZOATE | 0.025% | 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 |
|---|---|---|---|---|---|---|---|
| 06/28/1974 | ORIG-1 | Approval | Type 3 - New Dosage Form | STANDARD |
Label is not available on this site. |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 03/13/1981 | SUPPL-9 | Labeling |
Label is not available on this site. |
||
| 11/21/1978 | SUPPL-7 | Labeling |
Label is not available on this site. |
||
| 12/13/1974 | SUPPL-4 | Labeling |
Label is not available on this site. |