Package 63629-2400-1

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 63629-2400-1
Digits Only 6362924001
Product NDC 63629-2400
Description

1000 TABLET in 1 BOTTLE (63629-2400-1)

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": "b0b54e62-3b4a-4728-9ae2-198cfdc818ac", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198086"], "spl_set_id": ["ee6c3196-becf-439d-9e22-70d82bd94365"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-2400-1)", "package_ndc": "63629-2400-1", "marketing_start_date": "20210223"}], "brand_name": "Phenobarbital", "product_id": "63629-2400_b0b54e62-3b4a-4728-9ae2-198cfdc818ac", "dosage_form": "TABLET", "product_ndc": "63629-2400", "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"}