Package 71335-1245-8
Brand: oxycodone hydrochloride
Generic: oxycodone hydrochloridePackage Facts
Identity
Package NDC
71335-1245-8
Digits Only
7133512458
Product NDC
71335-1245
Description
28 TABLET in 1 BOTTLE (71335-1245-8)
Marketing
Marketing Status
Brand
oxycodone hydrochloride
Generic
oxycodone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a22286fc-994f-48fb-b106-0de005e83d94", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049618"], "spl_set_id": ["685d9709-028e-4422-bf0c-fde577b718a2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1245-1)", "package_ndc": "71335-1245-1", "marketing_start_date": "20190920"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1245-2)", "package_ndc": "71335-1245-2", "marketing_start_date": "20190528"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1245-3)", "package_ndc": "71335-1245-3", "marketing_start_date": "20240709"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1245-4)", "package_ndc": "71335-1245-4", "marketing_start_date": "20190708"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1245-5)", "package_ndc": "71335-1245-5", "marketing_start_date": "20240709"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-1245-6)", "package_ndc": "71335-1245-6", "marketing_start_date": "20240709"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-1245-7)", "package_ndc": "71335-1245-7", "marketing_start_date": "20240709"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-1245-8)", "package_ndc": "71335-1245-8", "marketing_start_date": "20240709"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "71335-1245_a22286fc-994f-48fb-b106-0de005e83d94", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-1245", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_start_date": "20131018", "listing_expiration_date": "20261231"}