# SUAVECITO 5% Minoxidil Solution

NDC: 74866-414
Generic name: MINOXIDIL
Labeler / Manufacturer: SUAVECITO, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LIQUID
Routes: TOPICAL
Marketing started: 20230731

FDA application: ANDA076239

## 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:"74866-414"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=74866-414
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a6d3c488-f943-4edf-9d6b-21a3dee92d78