# minoxidil topical

NDC: 59640-000
Generic name: Minoxidil
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: TOPICAL
Marketing started: 20211231

FDA application: ANDA075357

## Active ingredients

- MINOXIDIL: 2 g/100mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59640-000"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59640-000
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c9da0a80-2737-4e36-bbef-f7c4ae046ad7