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Sodium Phenylacetate and Sodium Benzoate

NDC 72266-236 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerFOSUN PHARMA USA INC
Marketing categoryNew Drug Application (innovator) · App NDA215025
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsSODIUM BENZOATE (100 mg/mL)
SODIUM PHENYLACETATE (100 mg/mL)
Marketing started20211114
Package count1

External sources

Source: openFDA. Public-domain (CC0).