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SODIUM PHENYLACETATE AND SODIUM BENZOATE

NDC 70511-101 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Generic namesodium phenylacetate and sodium benzoate
Labeler / ManufacturerMAIA PHARMACEUTICALS, INC
Marketing categoryAbbreviated NDA (generic) · App ANDA208521
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsSODIUM BENZOATE (100 mg/mL)
SODIUM PHENYLACETATE (100 mg/mL)
Marketing started20170522
Package count1

External sources

Source: openFDA. Public-domain (CC0).