# Minoxidil

NDC: 0591-5643
Generic name: Minoxidil
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20091026

FDA application: ANDA071345

## Active ingredients

- MINOXIDIL: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0591-5643"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0591-5643
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ab30461c-f8c8-409d-9e24-d58ed8a34873