# Sodium phenylbutyrate

NDC: 68475-011
Generic name: Sodium phenylbutyrate
Labeler / Manufacturer: Navinta LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260710

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:"68475-011"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68475-011
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c564778d-b285-4d1d-a641-9d4ee76079cf