Package 63629-2044-1

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 63629-2044-1
Digits Only 6362920441
Product NDC 63629-2044
Description

500 TABLET in 1 BOTTLE (63629-2044-1)

Marketing

Marketing Status
Marketed Since 2020-03-01
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": "6f577147-d9ce-4cda-82ff-e2545761153b", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["312362"], "spl_set_id": ["0f44f198-dafe-4c3b-bc01-91a71a825a11"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-2044-1)", "package_ndc": "63629-2044-1", "marketing_start_date": "20200301"}], "brand_name": "Phenobarbital", "product_id": "63629-2044_6f577147-d9ce-4cda-82ff-e2545761153b", "dosage_form": "TABLET", "product_ndc": "63629-2044", "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": "30 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}