# Minoxidil

NDC: 72162-1490
Generic name: Minoxidil
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19881114

FDA application: ANDA071839

## Active ingredients

- MINOXIDIL: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-1490"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-1490
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=665cba3d-5f26-468a-a047-188a413fbede