# Sodium Phenylacetate and Sodium Benzoate

NDC: 72266-236
Generic name: Sodium Phenylacetate and Sodium Benzoate
Labeler / Manufacturer: FOSUN PHARMA USA INC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20211114

FDA application: NDA215025

## Active ingredients

- SODIUM BENZOATE: 100 mg/mL
- SODIUM PHENYLACETATE: 100 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72266-236"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72266-236
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cee1e9a2-bbe5-2419-e053-2a95a90ac3ef