Package 71335-1080-9
Brand: oxycodone hydrochloride
Generic: oxycodonePackage Facts
Identity
Package NDC
71335-1080-9
Digits Only
7133510809
Product NDC
71335-1080
Description
18 TABLET in 1 BOTTLE (71335-1080-9)
Marketing
Marketing Status
Brand
oxycodone hydrochloride
Generic
oxycodone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b195b697-0b1f-4ed8-9ebf-21bb6c0bd552", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611"], "spl_set_id": ["d248ceba-9492-4348-aa07-31c9c73a3620"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1080-1)", "package_ndc": "71335-1080-1", "marketing_start_date": "20190129"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1080-2)", "package_ndc": "71335-1080-2", "marketing_start_date": "20190129"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1080-3)", "package_ndc": "71335-1080-3", "marketing_start_date": "20190215"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1080-4)", "package_ndc": "71335-1080-4", "marketing_start_date": "20190507"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1080-5)", "package_ndc": "71335-1080-5", "marketing_start_date": "20240530"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE (71335-1080-6)", "package_ndc": "71335-1080-6", "marketing_start_date": "20240530"}, {"sample": false, "description": "84 TABLET in 1 BOTTLE (71335-1080-7)", "package_ndc": "71335-1080-7", "marketing_start_date": "20240530"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-1080-8)", "package_ndc": "71335-1080-8", "marketing_start_date": "20240530"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-1080-9)", "package_ndc": "71335-1080-9", "marketing_start_date": "20240530"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "71335-1080_b195b697-0b1f-4ed8-9ebf-21bb6c0bd552", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-1080", "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": "15 mg/1"}], "application_number": "ANDA203638", "marketing_category": "ANDA", "marketing_start_date": "20121030", "listing_expiration_date": "20261231"}