# MINOXIDIL

NDC: 63629-1086
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: 19951214

FDA application: ANDA072709

## Active ingredients

- MINOXIDIL: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63629-1086"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-1086
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=40da3ec5-39db-42f1-b0d6-39d852130307