# Regoxidine (For Women)

NDC: 57483-540
Generic name: Minoxidil
Labeler / Manufacturer: Innovus Pharmaceuticals, 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:"57483-540"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57483-540
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b60cc177-700c-4007-be1a-2cb74824e657