Package 69367-625-01

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 69367-625-01
Digits Only 6936762501
Product NDC 69367-625
Description

100 TABLET in 1 BOTTLE (69367-625-01)

Marketing

Marketing Status
Marketed Since 2023-09-08
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": "d27572eb-a595-4050-a278-6a219541ad67", "openfda": {"upc": ["0369367627016", "0369367625012", "0369367626019", "0369367628013"], "unii": ["YQE403BP4D"], "rxcui": ["198086", "199164", "199167", "199168"], "spl_set_id": ["f8ba853a-d699-4a91-a23d-9ac9b9dbe69a"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-625-01)", "package_ndc": "69367-625-01", "marketing_start_date": "20230908"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69367-625-10)", "package_ndc": "69367-625-10", "marketing_start_date": "20230908"}], "brand_name": "Phenobarbital", "product_id": "69367-625_d27572eb-a595-4050-a278-6a219541ad67", "dosage_form": "TABLET", "product_ndc": "69367-625", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Westminster Pharmaceuticals, LLC", "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": "20230908", "listing_expiration_date": "20261231"}