# Minoxidil

NDC: 0363-9971
Generic name: Minoxidil
Labeler / Manufacturer: Walgreens
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: TOPICAL
Marketing started: 20221014

FDA application: ANDA075518

## Active ingredients

- MINOXIDIL: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0363-9971"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-9971
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=97d4d3ce-316c-4d58-b4dc-28d662b0fb4a