# Minoxidil

NDC: 68071-3794
Generic name: Minoxidil
Labeler / Manufacturer: NuCare Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19881114

FDA application: ANDA071826

## 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:"68071-3794"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3794
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2e5a2976-06fb-43f9-e063-6294a90a3bf5