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Sodium Acetate

NDC 71357-007 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerMILLA PHARMACEUTICALS INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA214805
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsSODIUM ACETATE (164 mg/mL)
Marketing started20241025
Package count1

External sources

Source: openFDA. Public-domain (CC0).