Minoxidil (For Women), Minoxidil (For Men)

ANDA 74743, held by Sight Pharms. Minoxidil.

As of Nov 15, 2026, ANDA 74743 (Minoxidil (For Women), Minoxidil (For Men)), held by Sight Pharms, was first approved by FDA on Oct 18, 1996, with 2 approved supplements and 0 published complete response letters.

First approved: Oct 18, 1996
Supplements approved: 2
Complete response letters: 0

Approvals and New Uses

The original application and every efficacy supplement, newest first; all 3 submissions below

Date	Submission	Status	Documents
Oct 18, 1996	Original application	Approved	None posted

Products

2 strengths and forms


Minoxidil (For Women)2% · solution;topical	Minoxidil	Discontinued
Minoxidil (For Men)2% · solution;topical	Minoxidil	Discontinued

All 3 submissions, including labeling and manufacturing supplements


Mar 31, 1999	Supplement 3Manufacturing	Approved	None posted
Jul 22, 1997	Supplement 2Manufacturing	Approved	None posted
Oct 18, 1996	Original application	Approved	None posted

Identifiers

Application: ANDA 74743
Drugs@FDA: Overview at FDA
Company: SIGHT Pharms

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