Capitrol

NDA 17594, held by Westwood Squibb. Chloroxine.

As of Nov 13, 2026, NDA 17594 (Capitrol), held by Westwood Squibb, was first approved by FDA on Oct 19, 1976, with 15 approved supplements and 0 published complete response letters.

First approved: Oct 19, 1976
Review: Standard
Supplements approved: 15
Complete response letters: 0

Approvals and New Uses

The original application and every efficacy supplement, newest first; all 16 submissions below

Date	Submission	Status	Documents
Oct 19, 1976	Original applicationNew molecular entity · Standard review	Approved	None posted

Products

1 strengths and forms

Product	Active ingredient	Marketing
Capitrol2% · shampoo;topical	Chloroxine	Discontinued

All 16 submissions, including labeling and manufacturing supplements


Feb 8, 1989	Supplement 18Manufacturing · Standard review	Approved	None posted
Aug 8, 1988	Supplement 15Manufacturing · Standard review	Approved	None posted
Sep 15, 1987	Supplement 14Manufacturing · Standard review	Approved	None posted
May 13, 1986	Supplement 13Manufacturing · Standard review	Approved	None posted
Feb 13, 1986	Supplement 12Manufacturing · Standard review	Approved	None posted
Nov 13, 1984	Supplement 8Labeling · Standard review	Approved	None posted
Oct 14, 1982	Supplement 10Manufacturing · Standard review	Approved	None posted
Mar 24, 1982	Supplement 9Manufacturing · Standard review	Approved	None posted
Jun 11, 1981	Supplement 6Manufacturing · Standard review	Approved	None posted
Jan 30, 1981	Supplement 7Manufacturing · Standard review	Approved	None posted
Jan 30, 1981	Supplement 3Manufacturing · Standard review	Approved	None posted
Aug 14, 1980	Supplement 5Manufacturing · Standard review	Approved	None posted
May 1, 1980	Supplement 4Manufacturing · Standard review	Approved	None posted
Apr 3, 1979	Supplement 2Manufacturing · Standard review	Approved	None posted
Apr 27, 1978	Supplement 1Labeling · Standard review	Approved	None posted
Oct 19, 1976	Original applicationNew molecular entity · Standard review	Approved	None posted

Identifiers

Application: NDA 17594
Drugs@FDA: Overview at FDA
Company: Westwood-Squibb Pharmaceuticals

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