# Minoxidil

NDC: 0363-9970
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: ANDA074588

## Active ingredients

- MINOXIDIL: 2 g/100mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0363-9970"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-9970
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b55198cb-40d8-432b-bdd5-2ecefa35d320