# Minoxidil Topical Solution 2%

NDC: 51672-2152
Generic name: Minoxidil Topical Solution 2%
Labeler / Manufacturer: SUN PHARMACEUTICAL INDUSTRIES, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: TOPICAL
Marketing started: 20250901

FDA application: ANDA218175

## Active ingredients

- MINOXIDIL: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-2152"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-2152
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=15d7cdd7-6d37-477c-bce7-a459ea960a53