# Minoxidil

NDC: 82804-240
Generic name: Minoxidil
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19881114

FDA application: ANDA071826

## Active ingredients

- MINOXIDIL: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82804-240"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-240
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a0066eac-cb58-49ef-a480-105cb1043c2b