Package 72189-375-30

{"route": ["ORAL"], "spl_id": "4c4c55ca-eef7-8b39-e063-6294a90adf3f", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049225"], "spl_set_id": ["e84245ca-957f-e85b-e053-2a95a90a836b"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-375-30)", "package_ndc": "72189-375-30", "marketing_start_date": "20220909"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-375-60)", "package_ndc": "72189-375-60", "marketing_start_date": "20220909"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (72189-375-72)", "package_ndc": "72189-375-72", "marketing_start_date": "20220909"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-375-90)", "package_ndc": "72189-375-90", "marketing_start_date": "20220909"}], "brand_name": "Oxycodone/APAP", "product_id": "72189-375_4c4c55ca-eef7-8b39-e063-6294a90adf3f", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-375", "dea_schedule": "CII", "generic_name": "Oxycodone/APAP", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone/APAP", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA201278", "marketing_category": "ANDA", "marketing_start_date": "20220909", "listing_expiration_date": "20271231"}