# MINOXIDIL

NDC: 53489-386
Generic name: minoxidil
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19951214

FDA application: ANDA072709

## Active ingredients

- MINOXIDIL: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53489-386"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53489-386
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0354a7f5-5917-44dc-9963-411104008cb5