Package 71335-1953-0

{"route": ["ORAL"], "spl_id": "1858e9af-6a66-478e-8db0-0723f439f7bd", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049225"], "spl_set_id": ["4da8a7bd-0d2e-452c-afb5-fed4e230a9bd"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "84 TABLET in 1 BOTTLE (71335-1953-0)", "package_ndc": "71335-1953-0", "marketing_start_date": "20221013"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1953-1)", "package_ndc": "71335-1953-1", "marketing_start_date": "20210929"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1953-2)", "package_ndc": "71335-1953-2", "marketing_start_date": "20210929"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1953-3)", "package_ndc": "71335-1953-3", "marketing_start_date": "20210917"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1953-4)", "package_ndc": "71335-1953-4", "marketing_start_date": "20211007"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1953-5)", "package_ndc": "71335-1953-5", "marketing_start_date": "20221013"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-1953-6)", "package_ndc": "71335-1953-6", "marketing_start_date": "20221013"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-1953-7)", "package_ndc": "71335-1953-7", "marketing_start_date": "20221013"}, {"sample": false, "description": "168 TABLET in 1 BOTTLE (71335-1953-8)", "package_ndc": "71335-1953-8", "marketing_start_date": "20221013"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1953-9)", "package_ndc": "71335-1953-9", "marketing_start_date": "20221013"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "71335-1953_1858e9af-6a66-478e-8db0-0723f439f7bd", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-1953", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}