FDA NDC Directory · JSON-LD · Markdown

acetaZOLAMIDE

NDC 70710-1239 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211069
Dosage form / routeTABLET · ORAL
Active ingredientsACETAZOLAMIDE (250 mg/1)
Marketing started20230804
Package count1

External sources

Source: openFDA. Public-domain (CC0).