# Sodium phenylbutyrate

NDC: 70710-2180
Generic name: Sodium phenylbutyrate
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260323

FDA application: ANDA220418

## Active ingredients

- SODIUM PHENYLBUTYRATE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-2180"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-2180
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d08fd548-7eb8-4f6f-b664-b0fff6f30065