Package 63629-2046-1

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 63629-2046-1
Digits Only 6362920461
Product NDC 63629-2046
Description

500 TABLET in 1 BOTTLE (63629-2046-1)

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": "53e6f8d0-42ef-4d1a-839f-8cc3e956650c", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198089"], "spl_set_id": ["b843ed58-ab59-4c21-b1b2-83749f1f8867"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-2046-1)", "package_ndc": "63629-2046-1", "marketing_start_date": "20200301"}], "brand_name": "Phenobarbital", "product_id": "63629-2046_53e6f8d0-42ef-4d1a-839f-8cc3e956650c", "dosage_form": "TABLET", "product_ndc": "63629-2046", "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": "60 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}