Package 72162-1168-0

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 72162-1168-0
Digits Only 7216211680
Product NDC 72162-1168
Product ID 72162-1168_10734a98-e252-4514-9cc4-afe27d8ee2d8
Description

1000 TABLET in 1 BOTTLE, PLASTIC (72162-1168-0)

Marketing

Marketing Status
Marketed Since 2001-12-01
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (1)

Phenobarbital ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "10734a98-e252-4514-9cc4-afe27d8ee2d8", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["199164"], "spl_set_id": ["1750cd18-13e5-4ee5-8b45-4e56ea4d5ba6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (72162-1168-0)", "package_ndc": "72162-1168-0", "marketing_start_date": "20011201"}], "brand_name": "Phenobarbital", "product_id": "72162-1168_10734a98-e252-4514-9cc4-afe27d8ee2d8", "dosage_form": "TABLET", "product_ndc": "72162-1168", "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": "97.2 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20011201", "listing_expiration_date": "20261231"}