Package 72189-614-90

Brand: oxycodone hcl

Generic: oxycodone hcl
NDC Package

Package Facts

Identity

Package NDC 72189-614-90
Digits Only 7218961490
Product NDC 72189-614
Description

90 TABLET in 1 BOTTLE (72189-614-90)

Marketing

Marketing Status
Marketed Since 2025-04-07
Brand oxycodone hcl
Generic oxycodone hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "324575ed-d3d7-1b45-e063-6294a90aec0e", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611"], "spl_set_id": ["32323565-5add-96a9-e063-6294a90a5b4e"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-614-30)", "package_ndc": "72189-614-30", "marketing_start_date": "20250407"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-614-60)", "package_ndc": "72189-614-60", "marketing_start_date": "20250407"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-614-90)", "package_ndc": "72189-614-90", "marketing_start_date": "20250407"}], "brand_name": "Oxycodone HCL", "product_id": "72189-614_324575ed-d3d7-1b45-e063-6294a90aec0e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-614", "dea_schedule": "CII", "generic_name": "Oxycodone HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone HCL", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA077712", "marketing_category": "ANDA", "marketing_start_date": "20250407", "listing_expiration_date": "20261231"}