# MINOXIDIL 5% (FOR MEN)

NDC: 21130-208
Generic name: MINOXIDIL
Labeler / Manufacturer: Better Living Brands, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: AEROSOL, FOAM
Routes: TOPICAL
Marketing started: 20260703

FDA application: ANDA218616

## Active ingredients

- MINOXIDIL: 50 mg/g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"21130-208"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-208
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=53e33414-2aa4-3dbd-e063-6294a90a06b5