Package 72162-1267-0

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 72162-1267-0
Digits Only 7216212670
Product NDC 72162-1267
Description

1000 TABLET in 1 BOTTLE (72162-1267-0)

Marketing

Marketing Status
Marketed Since 2023-10-06
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (0)

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"}