# Sodium phenylacetate and Sodium benzoate

NDC: 70710-1926
Generic name: Sodium phenylacetate and Sodium benzoate
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20230919

FDA application: ANDA217526

## 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:"70710-1926"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1926
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0f17c50f-3761-4470-bf3b-63837a287b8a