# Minoxidil (For Women)

NDC: 11673-158
Generic name: Minoxidil
Labeler / Manufacturer: TARGET Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: AEROSOL, FOAM
Routes: TOPICAL
Marketing started: 20220816

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:"11673-158"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-158
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3a6bef39-1d8e-4ce3-9484-becd294566da