Package 61919-871-72

{"route": ["ORAL"], "spl_id": "3a85db26-4c30-c5dc-e063-6294a90ac2a2", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214"], "spl_set_id": ["90a11364-fc42-e94e-e053-2a95a90a9782"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (61919-871-60)", "package_ndc": "61919-871-60", "marketing_start_date": "20190821"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (61919-871-72)", "package_ndc": "61919-871-72", "marketing_start_date": "20190821"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "61919-871_3a85db26-4c30-c5dc-e063-6294a90ac2a2", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "61919-871", "dea_schedule": "CII", "generic_name": "OXYCODONE AND ACETAMINOPHEN", "labeler_name": "Direct_Rx", "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": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20190821", "listing_expiration_date": "20261231"}