# Minoxidil For Women

NDC: 51672-2129
Generic name: Minoxidil
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: AEROSOL, FOAM
Routes: TOPICAL
Marketing started: 20190422

FDA application: ANDA209074

## Active ingredients

- MINOXIDIL: 50 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-2129"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-2129
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=82d7a480-46b2-423b-8da0-a4fc252f7747