FDA NDC Directory · JSON-LD · Markdown

Acetazolamide

NDC 72789-045 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209734
Dosage form / routeTABLET · ORAL
Active ingredientsACETAZOLAMIDE (125 mg/1)
Marketing started20171120
Package count2

External sources

Source: openFDA. Public-domain (CC0).