FDA NDC Directory · JSON-LD · Markdown

Acetazolamide

NDC 72789-237 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211556
Dosage form / routeTABLET · ORAL
Active ingredientsACETAZOLAMIDE (250 mg/1)
Marketing started20200130
Package count1

External sources

Source: openFDA. Public-domain (CC0).