Package 72162-1166-0

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 72162-1166-0
Digits Only 7216211660
Product NDC 72162-1166
Description

1000 TABLET in 1 BOTTLE, PLASTIC (72162-1166-0)

Marketing

Marketing Status
Marketed Since 2002-03-01
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": "958d3a1f-80f7-4b60-af07-3a9b81ceb872", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198086"], "spl_set_id": ["f85515e4-06cf-42d7-8e3e-066874787a04"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (72162-1166-0)", "package_ndc": "72162-1166-0", "marketing_start_date": "20020301"}], "brand_name": "Phenobarbital", "product_id": "72162-1166_958d3a1f-80f7-4b60-af07-3a9b81ceb872", "dosage_form": "TABLET", "product_ndc": "72162-1166", "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": "20020301", "listing_expiration_date": "20261231"}