United States · FDA National Drug Code directory
Pentobarbital Sodium
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
- 24201-010_092d00fe-9f8a-47ea-b9bc-07ef41d2b418
- Product NDC
- 24201-010
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Pentobarbital Sodium
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251001
- Source listing expiry
- 20271231
Source-listed ingredients
- PENTOBARBITAL SODIUM — 50 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (24201-010-20) / 20 mL in 1 VIAL · 24201-010-20
- 1 VIAL in 1 CARTON (24201-010-50) / 50 mL in 1 VIAL · 24201-010-50
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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