United States · FDA National Drug Code directory
Minoxidil (For Women)
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
- 82376-6007_78f0bcf6-b1b3-4f5b-a608-8f1fb0cfd2ca
- Product NDC
- 82376-6007
- Form
- AEROSOL, FOAM
- Composition / generic term
- Minoxidil
- Labeler
- SPAZI INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220830
- Source listing expiry
- 20261231
Source-listed ingredients
- MINOXIDIL — 50 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 2 CAN in 1 CARTON (82376-6007-2) / 60 g in 1 CAN (82376-6007-8) · 82376-6007-2
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 →