United States · FDA National Drug Code directory
Sodium phenylbutyrate
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
- 70710-2180_47ef97e0-8853-4254-b969-1a489764cec1
- Product NDC
- 70710-2180
- Form
- TABLET
- Composition / generic term
- Sodium phenylbutyrate
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260323
- Source listing expiry
- 20271231
Source-listed ingredients
- SODIUM PHENYLBUTYRATE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (70710-2180-8) / 250 TABLET in 1 BOTTLE · 70710-2180-8
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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