Package 72189-618-30

Brand: oxycodone hcl

Generic: oxycodone hcl
NDC Package

Package Facts

Identity

Package NDC 72189-618-30
Digits Only 7218961830
Product NDC 72189-618
Product ID 72189-618_3a851e5a-f061-4676-e063-6294a90ac16c
Description

30 TABLET in 1 BOTTLE (72189-618-30)

Marketing

Marketing Status
Marketed Since 2025-04-08
Brand oxycodone hcl
Generic oxycodone hcl
Sample Package No

Linked Drug Pages (1)

Oxycodone HCL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a851e5a-f061-4676-e063-6294a90ac16c", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["3245cd2f-8ad0-b755-e063-6394a90a603c"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-618-30)", "package_ndc": "72189-618-30", "marketing_start_date": "20250408"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-618-60)", "package_ndc": "72189-618-60", "marketing_start_date": "20250408"}], "brand_name": "Oxycodone HCL", "product_id": "72189-618_3a851e5a-f061-4676-e063-6294a90ac16c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-618", "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": "5 mg/1"}], "application_number": "ANDA077712", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}