FDA NDC Directory · JSON-LD · Markdown

methazolamide

NDC 0574-0791 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPadagis US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040062
Dosage form / routeTABLET · ORAL
Active ingredientsMETHAZOLAMIDE (50 mg/1)
Marketing started20140930
Marketing ended20270930
Package count1

External sources

Source: openFDA. Public-domain (CC0).