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
75987-060_3178e0bc-ebb7-4ddd-be43-630ff87eeb02
Product NDC
75987-060
Form
TABLET
Composition / generic term
sodium phenylbutyrate
Labeler
Horizon Therapeutics USA, Inc.
Marketing category
NDA
Marketing start / end (source format)
19960513
Source listing expiry
20261231

Source-listed ingredients

  • SODIUM PHENYLBUTYRATE — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (75987-060-08) / 250 TABLET in 1 BOTTLE · 75987-060-08

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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