Package 72189-613-30

Brand: oxycodone hcl

Generic: oxycodone hcl
NDC Package

Package Facts

Identity

Package NDC 72189-613-30
Digits Only 7218961330
Product NDC 72189-613
Product ID 72189-613_323148b2-809b-db11-e063-6294a90abe36
Description

30 TABLET in 1 BOTTLE (72189-613-30)

Marketing

Marketing Status
Marketed Since 2025-04-07
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": "323148b2-809b-db11-e063-6294a90abe36", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049686"], "spl_set_id": ["323148b2-809a-db11-e063-6294a90abe36"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-613-30)", "package_ndc": "72189-613-30", "marketing_start_date": "20250407"}], "brand_name": "Oxycodone HCL", "product_id": "72189-613_323148b2-809b-db11-e063-6294a90abe36", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-613", "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": "20 mg/1"}], "application_number": "ANDA077712", "marketing_category": "ANDA", "marketing_start_date": "20250407", "listing_expiration_date": "20261231"}