# minoxidil

NDC: 0113-5129
Generic name: Minoxidil
Labeler / Manufacturer: L. Perrigo Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: AEROSOL, FOAM
Routes: TOPICAL
Marketing started: 20240308

FDA application: ANDA091344

## Active ingredients

- MINOXIDIL: 50 mg/g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0113-5129"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0113-5129
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ec91e5f2-f9c4-4a1d-a94c-3b7352339dab