Package 72162-1339-3

{"route": ["ORAL"], "spl_id": "34f3992d-31b6-2875-e063-6294a90ad33c", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214"], "spl_set_id": ["79c3af61-19e7-40e5-bd20-2cea52f0bd3a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72162-1339-3)", "package_ndc": "72162-1339-3", "marketing_start_date": "20250512"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (72162-1339-5)", "package_ndc": "72162-1339-5", "marketing_start_date": "20241224"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72162-1339-6)", "package_ndc": "72162-1339-6", "marketing_start_date": "20250512"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72162-1339-9)", "package_ndc": "72162-1339-9", "marketing_start_date": "20250512"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "72162-1339_34f3992d-31b6-2875-e063-6294a90ad33c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1339", "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": "10 mg/1"}], "application_number": "ANDA201278", "marketing_category": "ANDA", "marketing_start_date": "20140828", "listing_expiration_date": "20261231"}