Package 63629-2289-1

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 63629-2289-1
Digits Only 6362922891
Product NDC 63629-2289
Description

1000 TABLET in 1 BOTTLE, PLASTIC (63629-2289-1)

Marketing

Marketing Status
Marketed Since 2002-03-01
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": "7fb89656-6d68-4943-b682-7df5b242c49b", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198086"], "spl_set_id": ["b53fc65c-02f2-4a77-914c-8f2c78fca546"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (63629-2289-1)", "package_ndc": "63629-2289-1", "marketing_start_date": "20020301"}], "brand_name": "Phenobarbital", "product_id": "63629-2289_7fb89656-6d68-4943-b682-7df5b242c49b", "dosage_form": "TABLET", "product_ndc": "63629-2289", "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": "20020301", "listing_expiration_date": "20261231"}