# Regenpure Precision

NDC: 71290-813
Generic name: MINOXIDIL
Labeler / Manufacturer: Salonceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LIQUID
Routes: TOPICAL
Marketing started: 20170304

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:"71290-813"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71290-813
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4a113921-b2a9-42cc-e054-00144ff8d46c