FDA NDC Directory · JSON-LD · Markdown

MINOXIDIL

NDC 53489-387 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameminoxidil
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA072709
Dosage form / routeTABLET · ORAL
Active ingredientsMINOXIDIL (10 mg/1)
Marketing started19951214
Package count4

External sources

Source: openFDA. Public-domain (CC0).