Package 72162-1265-1

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 72162-1265-1
Digits Only 7216212651
Product NDC 72162-1265
Product ID 72162-1265_0308bc99-4ace-43f0-9d40-cfef627ad1a8
Description

100 TABLET in 1 BOTTLE (72162-1265-1)

Marketing

Marketing Status
Marketed Since 2023-09-13
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (1)

Phenobarbital ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0308bc99-4ace-43f0-9d40-cfef627ad1a8", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["199168"], "spl_set_id": ["b099ff66-da3d-47a1-b721-8b5b5e4a13ba"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1265-0)", "package_ndc": "72162-1265-0", "marketing_start_date": "20230913"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1265-1)", "package_ndc": "72162-1265-1", "marketing_start_date": "20230913"}], "brand_name": "Phenobarbital", "product_id": "72162-1265_0308bc99-4ace-43f0-9d40-cfef627ad1a8", "dosage_form": "TABLET", "product_ndc": "72162-1265", "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": "64.8 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20201101", "listing_expiration_date": "20261231"}