Triamcinolone Acetonide

ANDA 87902, held by Sun Pharma Canada. Triamcinolone Acetonide.

As of Nov 15, 2026, ANDA 87902 (Triamcinolone Acetonide), held by Sun Pharma Canada, was first approved by FDA on Dec 27, 1982, with 19 approved supplements and 0 published complete response letters.

First approved: Dec 27, 1982
Supplements approved: 19
Complete response letters: 0

Approvals and New Uses

The original application and every efficacy supplement, newest first; all 20 submissions below

Date	Submission	Status	Documents
Dec 27, 1982	Original application	Approved	None posted

Products

1 strengths and forms

Product	Active ingredient	Marketing
Triamcinolone Acetonide0.1% · ointment;topical	Triamcinolone Acetonide	Discontinued

All 20 submissions, including labeling and manufacturing supplements


Apr 8, 1993	Supplement 31Labeling	Approved	None posted
Nov 16, 1992	Supplement 30Labeling	Approved	None posted
Oct 28, 1991	Supplement 29Labeling	Approved	None posted
Mar 5, 1991	Supplement 28Labeling	Approved	None posted
Aug 6, 1990	Supplement 25Labeling	Approved	None posted
Mar 28, 1990	Supplement 19Manufacturing	Approved	None posted
Mar 1, 1990	Supplement 24Labeling	Approved	None posted
Jan 22, 1990	Supplement 18Manufacturing	Approved	None posted
Jan 22, 1990	Supplement 22Manufacturing	Approved	None posted
Nov 21, 1989	Supplement 23Labeling	Approved	None posted
Mar 2, 1989	Supplement 21Labeling	Approved	None posted
Feb 7, 1989	Supplement 20Labeling	Approved	None posted
Apr 21, 1988	Supplement 16Labeling	Approved	None posted
Sep 15, 1987	Supplement 15Manufacturing	Approved	None posted
Sep 8, 1987	Supplement 12Manufacturing	Approved	None posted
Jan 30, 1986	Supplement 9Manufacturing	Approved	None posted
Dec 3, 1985	Supplement 7Manufacturing	Approved	None posted
Jun 14, 1984	Supplement 2Manufacturing	Approved	None posted
Jun 14, 1984	Supplement 3Manufacturing	Approved	None posted
Dec 27, 1982	Original application	Approved	None posted

Identifiers

Application: ANDA 87902
Drugs@FDA: Overview at FDA
Company: Sun Pharma Canada

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