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Acetazolamide

NDC 72888-048 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvagen Pharma Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA215101
Dosage form / routeTABLET · ORAL
Active ingredientsACETAZOLAMIDE (250 mg/1)
Marketing started20210819
Package count1

External sources

Source: openFDA. Public-domain (CC0).