Package 16571-669-01

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 16571-669-01
Digits Only 1657166901
Product NDC 16571-669
Description

100 TABLET in 1 BOTTLE (16571-669-01)

Marketing

Marketing Status
Marketed Since 2020-11-01
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": "e81ffc2f-9aa0-4b68-9d42-63d23dc30824", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198083", "198089", "312357", "312362"], "spl_set_id": ["e81ffc2f-9aa0-4b68-9d42-63d23dc30824"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-669-01)", "package_ndc": "16571-669-01", "marketing_start_date": "20201101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (16571-669-10)", "package_ndc": "16571-669-10", "marketing_start_date": "20201101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16571-669-50)", "package_ndc": "16571-669-50", "marketing_start_date": "20201101"}], "brand_name": "Phenobarbital", "product_id": "16571-669_e81ffc2f-9aa0-4b68-9d42-63d23dc30824", "dosage_form": "TABLET", "product_ndc": "16571-669", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "100 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20201101", "listing_expiration_date": "20261231"}