Package 72162-1812-0

Brand: oxycodone hydrochloride

Generic: oxycodone
NDC Package

Package Facts

Identity

Package NDC 72162-1812-0
Digits Only 7216218120
Product NDC 72162-1812
Product ID 72162-1812_76f5ec67-3129-4514-b9fa-fd389c57a216
Description

60 TABLET in 1 BOTTLE (72162-1812-0)

Marketing

Marketing Status
Marketed Since 2024-05-30
Brand oxycodone hydrochloride
Generic oxycodone
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "76f5ec67-3129-4514-b9fa-fd389c57a216", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049618"], "spl_set_id": ["232d44d2-3924-4d35-873c-d2aef75e9a41"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-1812-0)", "package_ndc": "72162-1812-0", "marketing_start_date": "20240530"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-1812-1)", "package_ndc": "72162-1812-1", "marketing_start_date": "20240530"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "72162-1812_76f5ec67-3129-4514-b9fa-fd389c57a216", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1812", "dea_schedule": "CII", "generic_name": "Oxycodone", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA203638", "marketing_category": "ANDA", "marketing_start_date": "20121030", "listing_expiration_date": "20261231"}