Triacet

ANDA 84908, held by Teva. Triamcinolone Acetonide.

As of Nov 15, 2026, ANDA 84908 (Triacet), held by Teva, was first approved by FDA on May 24, 1976, with 23 approved supplements and 0 published complete response letters.

First approved: May 24, 1976
Supplements approved: 23
Complete response letters: 0

Approvals and New Uses

The original application and every efficacy supplement, newest first; all 24 submissions below

Date	Submission	Status	Documents
May 24, 1976	Original application	Approved	None posted

Products

3 strengths and forms


Triacet0.025% · cream;topical	Triamcinolone Acetonide	Discontinued
Triacet0.1% · cream;topical	Triamcinolone Acetonide	Discontinued
Triacet0.5% · cream;topical	Triamcinolone Acetonide	Discontinued

All 24 submissions, including labeling and manufacturing supplements


Aug 30, 2001	Supplement 57Manufacturing	Approved	None posted
Jul 7, 2000	Supplement 56Manufacturing	Approved	None posted
Feb 17, 2000	Supplement 55Manufacturing	Approved	None posted
Jun 13, 1996	Supplement 54Manufacturing	Approved	None posted
May 4, 1995	Supplement 53Manufacturing	Approved	None posted
May 4, 1995	Supplement 52Manufacturing	Approved	None posted
May 9, 1994	Supplement 44Manufacturing	Approved	None posted
Jan 13, 1994	Supplement 51Manufacturing	Approved	None posted
Aug 31, 1993	Supplement 50Manufacturing	Approved	None posted
Aug 31, 1993	Supplement 49Manufacturing	Approved	None posted
Aug 31, 1993	Supplement 48Manufacturing	Approved	None posted
Aug 31, 1993	Supplement 47Manufacturing	Approved	None posted
Apr 1, 1993	Supplement 45Manufacturing	Approved	None posted
Mar 10, 1993	Supplement 46Labeling	Approved	None posted
Jun 28, 1989	Supplement 43Manufacturing	Approved	None posted
Sep 2, 1988	Supplement 42Manufacturing	Approved	None posted
Jan 29, 1985	Supplement 39Manufacturing	Approved	None posted
Apr 22, 1983	Supplement 36Manufacturing	Approved	None posted
Jan 31, 1983	Supplement 35Manufacturing	Approved	None posted
Jan 31, 1983	Supplement 30Manufacturing	Approved	None posted
Oct 15, 1982	Supplement 32Manufacturing	Approved	None posted
Oct 15, 1982	Supplement 31Manufacturing	Approved	None posted
Jun 7, 1982	Supplement 34Manufacturing	Approved	None posted
May 24, 1976	Original application	Approved	None posted

Identifiers

Application: ANDA 84908
Drugs@FDA: Overview at FDA
Company: Teva Pharmaceutical Industries

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