FDA NDC Directory · JSON-LD · Markdown

Acetazolamide

NDC 51672-4022 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040195
Dosage form / routeTABLET · ORAL
Active ingredientsACETAZOLAMIDE (125 mg/1)
Marketing started19970528
Package count1

External sources

Source: openFDA. Public-domain (CC0).