Package 72162-1337-3

{"route": ["ORAL"], "spl_id": "10c5dede-e7d3-48aa-a9e7-2c7e0d07a20c", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049618"], "spl_set_id": ["22f9eeaa-8aad-44f6-8258-e41edb60f876"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1337-3)", "package_ndc": "72162-1337-3", "marketing_start_date": "20240408"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72162-1337-6)", "package_ndc": "72162-1337-6", "marketing_start_date": "20240408"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-1337-9)", "package_ndc": "72162-1337-9", "marketing_start_date": "20240408"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "72162-1337_10c5dede-e7d3-48aa-a9e7-2c7e0d07a20c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1337", "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": "ANDA091490", "marketing_category": "ANDA", "marketing_start_date": "20140908", "listing_expiration_date": "20261231"}