FDA NDC Directory · JSON-LD · Markdown

Minoxidil

NDC 0591-5643 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerActavis Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA071345
Dosage form / routeTABLET · ORAL
Active ingredientsMINOXIDIL (10 mg/1)
Marketing started20091026
Package count2

External sources

Source: openFDA. Public-domain (CC0).