# Pentobarbital Sodium

NDC: 24201-010
Generic name: Pentobarbital Sodium
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20251001

FDA application: ANDA203619

## Active ingredients

- PENTOBARBITAL SODIUM: 50 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24201-010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24201-010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d375b92a-baa1-4d63-9ad1-1467dcfde7d5