FDA NDC Directory · JSON-LD · Markdown

Regenpure Precision

NDC 71290-813 · HUMAN OTC DRUG · LIQUID

Generic nameMINOXIDIL
Labeler / ManufacturerSalonceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076239
Dosage form / routeLIQUID · TOPICAL
Active ingredientsMINOXIDIL (50 mg/mL)
Marketing started20170304
Package count1

External sources

Source: openFDA. Public-domain (CC0).