FDA NDC Directory · JSON-LD · Markdown

METHAZOLAMIDE

NDC 42571-239 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameMethazolamide
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA207438
Dosage form / routeTABLET · ORAL
Active ingredientsMETHAZOLAMIDE (25 mg/1)
Marketing started20190305
Package count3

External sources

Source: openFDA. Public-domain (CC0).