United States · FDA National Drug Code directory

Womens Minoxidil Hair Growth System

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
51326-161_b2a7381d-b3ed-4db7-b7eb-06a3894ae34b
Product NDC
51326-161
Form
LIQUID
Composition / generic term
Minoxidil
Labeler
Topiderm, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20210326
Source listing expiry
20261231

Source-listed ingredients

  • MINOXIDIL — 20 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 mL in 1 BOTTLE (51326-161-01) · 51326-161-01

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →