# Minoxidil 5% (For Men)

NDC: 71713-091
Generic name: Minoxidil
Labeler / Manufacturer: Thirty MADISON, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: AEROSOL, FOAM
Routes: TOPICAL
Marketing started: 20220323

FDA application: ANDA209074

## Active ingredients

- MINOXIDIL: 50 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71713-091"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71713-091
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=985ba944-147c-4207-b34b-ede702c3d704