Package 63629-1033-1

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 63629-1033-1
Digits Only 6362910331
Product NDC 63629-1033
Description

1000 TABLET in 1 BOTTLE (63629-1033-1)

Marketing

Marketing Status
Marketed Since 2014-11-24
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": "27b391a3-b031-4b8a-9164-aee436aeac1f", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198086"], "spl_set_id": ["4477d357-112c-4205-b359-5ee89c4bf7d6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-1033-1)", "package_ndc": "63629-1033-1", "marketing_start_date": "20141124"}], "brand_name": "Phenobarbital", "product_id": "63629-1033_27b391a3-b031-4b8a-9164-aee436aeac1f", "dosage_form": "TABLET", "product_ndc": "63629-1033", "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": "20141124", "listing_expiration_date": "20261231"}