Package 63629-2401-1

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 63629-2401-1
Digits Only 6362924011
Product NDC 63629-2401
Description

100 TABLET in 1 BOTTLE (63629-2401-1)

Marketing

Marketing Status
Marketed Since 2021-02-23
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": "5500b038-6256-4d72-9ca3-a94d2a9dd664", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198086"], "spl_set_id": ["e1709a49-ee44-4679-9a57-a7ea85a78ab7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-2401-1)", "package_ndc": "63629-2401-1", "marketing_start_date": "20210223"}], "brand_name": "Phenobarbital", "product_id": "63629-2401_5500b038-6256-4d72-9ca3-a94d2a9dd664", "dosage_form": "TABLET", "product_ndc": "63629-2401", "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"}