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SODIUM ACETATE

NDC 80830-2437 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Generic namesodium acetate
Labeler / ManufacturerAmneal Pharmaceuticals Private Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218469
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsSODIUM ACETATE ANHYDROUS (164 mg/mL)
Marketing started20250812
Package count1

External sources

Source: openFDA. Public-domain (CC0).