FDA NDC Directory · JSON-LD · Markdown

Minoxidil For Women

NDC 51672-2129 · HUMAN OTC DRUG · AEROSOL, FOAM

Generic nameMinoxidil
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209074
Dosage form / routeAEROSOL, FOAM · TOPICAL
Active ingredientsMINOXIDIL (50 mg/g)
Marketing started20190422
Package count2

External sources

Source: openFDA. Public-domain (CC0).