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
71713-094_5a5f7ff1-cae3-4282-9a66-2453a4895bbe
Product NDC
71713-094
Form
SOLUTION
Composition / generic term
minoxidil
Labeler
THIRTY MADISON INC
Marketing category
ANDA
Marketing start / end (source format)
20220505
Source listing expiry
20261231

Source-listed ingredients

  • MINOXIDIL — 5 g/100mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 3 BOTTLE, DROPPER in 1 CARTON (71713-094-30) / 60 mL in 1 BOTTLE, DROPPER (71713-094-16) · 71713-094-30

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.

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