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Sodium Phenylacetate and sodium benzoate

NDC 68475-001 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION, CONCENTRATE

Labeler / ManufacturerNavinta LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205880
Dosage form / routeINJECTION, SOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsSODIUM BENZOATE (100 mg/mL)
SODIUM PHENYLACETATE (100 mg/mL)
Marketing started20210304
Package count1

External sources

Source: openFDA. Public-domain (CC0).