# Minoxidil

NDC: 59726-122
Generic name: Minoxidil
Labeler / Manufacturer: P & L Development, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: AEROSOL, FOAM
Routes: TOPICAL
Marketing started: 20240531

FDA application: ANDA208092

## 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:"59726-122"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59726-122
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=204bab15-47c5-449c-a889-700914b04b61