Package 24201-010-50
Brand: pentobarbital sodium
Generic: pentobarbital sodiumPackage Facts
Identity
Package NDC
24201-010-50
Digits Only
2420101050
Product NDC
24201-010
Description
1 VIAL in 1 CARTON (24201-010-50) / 50 mL in 1 VIAL
Marketing
Marketing Status
Brand
pentobarbital sodium
Generic
pentobarbital sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "092d00fe-9f8a-47ea-b9bc-07ef41d2b418", "openfda": {"unii": ["NJJ0475N0S"], "rxcui": ["238090"], "spl_set_id": ["d375b92a-baa1-4d63-9ad1-1467dcfde7d5"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (24201-010-20) / 20 mL in 1 VIAL", "package_ndc": "24201-010-20", "marketing_start_date": "20251001"}, {"sample": false, "description": "1 VIAL in 1 CARTON (24201-010-50) / 50 mL in 1 VIAL", "package_ndc": "24201-010-50", "marketing_start_date": "20251001"}], "brand_name": "Pentobarbital Sodium", "product_id": "24201-010_092d00fe-9f8a-47ea-b9bc-07ef41d2b418", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "24201-010", "dea_schedule": "CII", "generic_name": "Pentobarbital Sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pentobarbital Sodium", "active_ingredients": [{"name": "PENTOBARBITAL SODIUM", "strength": "50 mg/mL"}], "application_number": "ANDA203619", "marketing_category": "ANDA", "marketing_start_date": "20251001", "listing_expiration_date": "20271231"}