Package 14789-127-05

Brand: phenobarbital sodium

Generic: phenobarbital sodium
NDC Package

Package Facts

Identity

Package NDC 14789-127-05
Digits Only 1478912705
Product NDC 14789-127
Description

10 VIAL, GLASS in 1 CARTON (14789-127-05) / 1 mL in 1 VIAL, GLASS (14789-127-07)

Marketing

Marketing Status
Marketed Since 2025-12-31
Brand phenobarbital sodium
Generic phenobarbital sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "45c7f956-27bd-dc6d-e063-6394a90a6181", "openfda": {"unii": ["SW9M9BB5K3"], "rxcui": ["2671204", "2671207"], "spl_set_id": ["472da201-698e-4d2b-8c53-595461d85bb6"], "manufacturer_name": ["Nexus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (14789-127-05)  / 1 mL in 1 VIAL, GLASS (14789-127-07)", "package_ndc": "14789-127-05", "marketing_start_date": "20251231"}], "brand_name": "Phenobarbital Sodium", "product_id": "14789-127_45c7f956-27bd-dc6d-e063-6394a90a6181", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "14789-127", "dea_schedule": "CIV", "generic_name": "Phenobarbital Sodium", "labeler_name": "Nexus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital Sodium", "active_ingredients": [{"name": "PHENOBARBITAL SODIUM", "strength": "65 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20231206", "listing_expiration_date": "20261231"}