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Pentobarbital Sodium

NDC 24201-010 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203619
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsPENTOBARBITAL SODIUM (50 mg/mL)
Marketing started20251001
Package count2

External sources

Source: openFDA. Public-domain (CC0).