# Buphenyl

NDC: 75987-070
Generic name: sodium phenylbutyrate
Labeler / Manufacturer: Horizon Therapeutics USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: POWDER
Routes: ORAL
Marketing started: 19960430

FDA application: NDA020573

## 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:"75987-070"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75987-070
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=463a36fa-3eb2-4326-8bd0-c8c7a11bca3a