# Minoxidil 5 Percent (For Women)

NDC: 70550-605
Generic name: Minoxidil
Labeler / Manufacturer: PROFECTUS BEAUTY LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: AEROSOL, FOAM
Routes: TOPICAL
Marketing started: 20220118

FDA application: ANDA209074

## Active ingredients

- MINOXIDIL: 50 mg/g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70550-605"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70550-605
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b307bcb7-4659-4dd7-86aa-00b3735f5844