United States · FDA National Drug Code directory
Buphenyl
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 75987-070_3178e0bc-ebb7-4ddd-be43-630ff87eeb02
- Product NDC
- 75987-070
- Form
- POWDER
- Composition / generic term
- sodium phenylbutyrate
- Labeler
- Horizon Therapeutics USA, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 19960430
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM PHENYLBUTYRATE — .94 g/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (75987-070-09) / 250 g in 1 BOTTLE · 75987-070-09
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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