# Sodium Phenylbutyrate

NDC: 42794-086
Generic name: Sodium Phenylbutyrate
Labeler / Manufacturer: Sigmapharm Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER
Routes: ORAL
Marketing started: 20130408

FDA application: ANDA202819

## Active ingredients

- SODIUM PHENYLBUTYRATE: .94 g/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42794-086"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42794-086
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e914d451-6122-43f9-af8d-c80ed1cb215d