Package 72162-1334-3

{"route": ["ORAL"], "spl_id": "990b08d3-98d8-43ca-b977-193f9c133126", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["7503ef9d-0fad-421f-951a-f35ab71f71c7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (72162-1334-2)", "package_ndc": "72162-1334-2", "marketing_start_date": "20240716"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1334-3)", "package_ndc": "72162-1334-3", "marketing_start_date": "20240716"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-1334-6)", "package_ndc": "72162-1334-6", "marketing_start_date": "20240716"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-1334-9)", "package_ndc": "72162-1334-9", "marketing_start_date": "20240716"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "72162-1334_990b08d3-98d8-43ca-b977-193f9c133126", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1334", "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": "5 mg/1"}], "application_number": "ANDA091490", "marketing_category": "ANDA", "marketing_start_date": "20140908", "listing_expiration_date": "20261231"}