Package 72189-632-30
Brand: oxycodone hcl
Generic: oxycodone hclPackage Facts
Identity
Package NDC
72189-632-30
Digits Only
7218963230
Product NDC
72189-632
Description
30 TABLET in 1 BOTTLE (72189-632-30)
Marketing
Marketing Status
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": "3a8579d0-8ea3-42bc-e063-6294a90a7fd2", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049683"], "spl_set_id": ["3a849aeb-b72c-5cde-e063-6394a90a9768"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-632-30)", "package_ndc": "72189-632-30", "marketing_start_date": "20250722"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-632-60)", "package_ndc": "72189-632-60", "marketing_start_date": "20250722"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-632-90)", "package_ndc": "72189-632-90", "marketing_start_date": "20250722"}], "brand_name": "Oxycodone HCL", "product_id": "72189-632_3a8579d0-8ea3-42bc-e063-6294a90a7fd2", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-632", "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": "10 mg/1"}], "application_number": "ANDA077712", "marketing_category": "ANDA", "marketing_start_date": "20250722", "listing_expiration_date": "20261231"}