# REGOXIDINE (FOR MEN)

NDC: 57483-165
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: 20250503

FDA application: ANDA218616

## 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:"57483-165"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57483-165
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d191b3a9-0fb7-45cc-82a1-b64a79c0c125