Package 72162-1584-1

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 72162-1584-1
Digits Only 7216215841
Product NDC 72162-1584
Description

100 TABLET in 1 BOTTLE, PLASTIC (72162-1584-1)

Marketing

Marketing Status
Marketed Since 2023-04-21
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": "04275a50-1692-9977-e063-6294a90a7efe", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198083"], "spl_set_id": ["97bab152-6c7b-4eb6-b8cc-9f64d2a5bdbe"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1584-1)", "package_ndc": "72162-1584-1", "marketing_start_date": "20230421"}], "brand_name": "Phenobarbital", "product_id": "72162-1584_04275a50-1692-9977-e063-6294a90a7efe", "dosage_form": "TABLET", "product_ndc": "72162-1584", "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": "100 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}