Pentobarbital Sodium
NDC 24201-010, Pentobarbital Sodium, injection, solution, from Hikma Pharmaceuticals USA Inc..
- Product NDC
- 24201-010
- Status
- Listed
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR, INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA203619
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/24201-010 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PENTOBARBITAL SODIUM50 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 24201-010-20 | 24201001020 | 1 VIAL in 1 CARTON (24201-010-20) / 20 mL in 1 VIAL |
| 24201-010-50 | 24201001050 | 1 VIAL in 1 CARTON (24201-010-50) / 50 mL in 1 VIAL |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/d375b92a-baa1-4d63-9ad1-1467dcfde7d5
Use it
Look up 24201-010 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/24201-010 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 24201-010. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.