Package 72162-1267-1
Brand: phenobarbital
Generic: phenobarbitalPackage Facts
Identity
Package NDC
72162-1267-1
Digits Only
7216212671
Product NDC
72162-1267
Description
100 TABLET in 1 BOTTLE (72162-1267-1)
Marketing
Marketing Status
Brand
phenobarbital
Generic
phenobarbital
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7c1c85c9-6581-42f8-8e33-2cc4722934a7", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198086"], "spl_set_id": ["2c238b77-6806-44af-9a66-fd871eaddfc0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1267-0)", "package_ndc": "72162-1267-0", "marketing_start_date": "20231006"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1267-1)", "package_ndc": "72162-1267-1", "marketing_start_date": "20231006"}], "brand_name": "Phenobarbital", "product_id": "72162-1267_7c1c85c9-6581-42f8-8e33-2cc4722934a7", "dosage_form": "TABLET", "product_ndc": "72162-1267", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "16.2 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20201101", "listing_expiration_date": "20261231"}