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Acetazolamide

NDC 72078-092 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameacetazolamide sodium
Labeler / ManufacturerMylan Institutional LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA200880
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsACETAZOLAMIDE SODIUM (500 mg/5mL)
Marketing started20260901
Package count1

External sources

Source: openFDA. Public-domain (CC0).