ANDA 87799, held by Actavis Mid Atlantic. Triamcinolone Acetonide.
As of Nov 15, 2026, ANDA 87799 (Triamcinolone Acetonide), held by Actavis Mid Atlantic, was first approved by FDA on Jun 7, 1982, with 15 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Jun 7, 1982 | Original application | Approved | None posted |
| Product | Active ingredient | Marketing |
|---|---|---|
| Triamcinolone Acetonide0.1% ยท ointment;topical | Triamcinolone Acetonide | Discontinued |
| May 30, 2001 | Supplement 17Manufacturing | Approved | None posted |
| Dec 29, 2000 | Supplement 16Manufacturing | Approved | None posted |
| Sep 10, 1996 | Supplement 11Manufacturing | Approved | None posted |
| Sep 10, 1996 | Supplement 12Manufacturing | Approved | None posted |
| Sep 10, 1996 | Supplement 13Manufacturing | Approved | None posted |
| Sep 10, 1996 | Supplement 15Manufacturing | Approved | None posted |
| Jun 28, 1996 | Supplement 14Manufacturing | Approved | None posted |
| Feb 7, 1996 | Supplement 10Manufacturing | Approved | None posted |
| Feb 3, 1995 | Supplement 8Manufacturing | Approved | None posted |
| Feb 3, 1995 | Supplement 9Manufacturing | Approved | None posted |
| Feb 19, 1991 | Supplement 5Labeling | Approved | None posted |
| Jul 26, 1989 | Supplement 6Manufacturing | Approved | None posted |
| Jul 26, 1989 | Supplement 7Manufacturing | Approved | None posted |
| Dec 20, 1985 | Supplement 3Manufacturing | Approved | None posted |
| Mar 8, 1983 | Supplement 2Manufacturing | Approved | None posted |
| Jun 7, 1982 | Original application | Approved | None posted |
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters
