United States · FDA National Drug Code directory

Minoxidil

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
0363-9971_b677fdb0-f980-4a2b-8af8-cbdc5c81770c
Product NDC
0363-9971
Form
SOLUTION
Composition / generic term
Minoxidil
Labeler
Walgreens
Marketing category
ANDA
Marketing start / end (source format)
20221014 / 20260928

Source-listed ingredients

  • MINOXIDIL — 50 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, DROPPER in 1 CARTON (0363-9971-02) / 60 mL in 1 BOTTLE, DROPPER · 0363-9971-02
  • 3 BOTTLE, DROPPER in 1 BOTTLE (0363-9971-06) / 60 mL in 1 BOTTLE, DROPPER · 0363-9971-06

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 →