Package 25021-676-50
Brand: pentobarbital sodium
Generic: pentobarbital sodiumPackage Facts
Identity
Package NDC
25021-676-50
Digits Only
2502167650
Product NDC
25021-676
Description
1 VIAL in 1 CARTON (25021-676-50) / 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": "5eb44748-b3d4-4d86-a172-9f03eb804671", "openfda": {"unii": ["NJJ0475N0S"], "rxcui": ["238090"], "spl_set_id": ["e9f4b344-b092-4eec-b49d-d8cfe8ebc05d"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-676-20) / 20 mL in 1 VIAL", "package_ndc": "25021-676-20", "marketing_start_date": "20170419"}, {"sample": false, "description": "1 VIAL in 1 CARTON (25021-676-50) / 50 mL in 1 VIAL", "package_ndc": "25021-676-50", "marketing_start_date": "20170419"}], "brand_name": "pentobarbital sodium", "product_id": "25021-676_5eb44748-b3d4-4d86-a172-9f03eb804671", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "25021-676", "dea_schedule": "CII", "generic_name": "pentobarbital sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "pentobarbital sodium", "active_ingredients": [{"name": "PENTOBARBITAL SODIUM", "strength": "50 mg/mL"}], "application_number": "ANDA206404", "marketing_category": "ANDA", "marketing_start_date": "20170419", "listing_expiration_date": "20261231"}