# Minoxidil Topical Solution, 5%

NDC: 51672-2151
Generic name: Minoxidil Solution
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: TOPICAL
Marketing started: 20250801

FDA application: ANDA217998

## Active ingredients

- MINOXIDIL: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-2151"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-2151
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=acc5ad74-4558-4be9-aab4-94ad9ddad6b2