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Acetazolamide

NDC 64380-834 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA209734
Dosage form / routeTABLET · ORAL
Active ingredientsACETAZOLAMIDE (250 mg/1)
Marketing started20171120
Package count2

External sources

Source: openFDA. Public-domain (CC0).