Package 72162-1811-1

Brand: oxycodone hydrochloride

Generic: oxycodone
NDC Package

Package Facts

Identity

Package NDC 72162-1811-1
Digits Only 7216218111
Product NDC 72162-1811
Product ID 72162-1811_c990c114-53b0-4621-9a31-c31ba43f6527
Description

60 TABLET in 1 BOTTLE (72162-1811-1)

Marketing

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

Linked Drug Pages (1)

Oxycodone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c990c114-53b0-4621-9a31-c31ba43f6527", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["bc7fdf7e-ad4e-4a04-b35c-2233cc7e5f15"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1811-0)", "package_ndc": "72162-1811-0", "marketing_start_date": "20240530"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-1811-1)", "package_ndc": "72162-1811-1", "marketing_start_date": "20240530"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-1811-2)", "package_ndc": "72162-1811-2", "marketing_start_date": "20240530"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "72162-1811_c990c114-53b0-4621-9a31-c31ba43f6527", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1811", "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": "5 mg/1"}], "application_number": "ANDA203638", "marketing_category": "ANDA", "marketing_start_date": "20121030", "listing_expiration_date": "20261231"}