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
- 59726-115_718a6b1f-b594-488d-8b9d-00891cb478f3
- Product NDC
- 59726-115
- Form
- AEROSOL, FOAM
- Composition / generic term
- Minoxidil
- Labeler
- P & L Development, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230505
- Source listing expiry
- 20261231
Source-listed ingredients
- MINOXIDIL — 50 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 60 g in 1 CAN (59726-115-60) · 59726-115-60
- 2 CAN in 1 PACKAGE (59726-115-65) / 60 g in 1 CAN · 59726-115-65
- 3 CAN in 1 PACKAGE (59726-115-70) / 60 g in 1 CAN · 59726-115-70
Source and coverage
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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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