Package 72189-256-30

{"route": ["ORAL"], "spl_id": "36d68732-0635-1380-e063-6394a90a69c6", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049225", "1049621", "1049683"], "spl_set_id": ["a8206207-ad09-83df-e053-2995a90a78b7"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-256-30)", "package_ndc": "72189-256-30", "marketing_start_date": "20210810"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-256-60)", "package_ndc": "72189-256-60", "marketing_start_date": "20210810"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (72189-256-72)", "package_ndc": "72189-256-72", "marketing_start_date": "20210810"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "72189-256_36d68732-0635-1380-e063-6394a90a69c6", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-256", "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": "7.5 mg/1"}], "application_number": "ANDA207510", "marketing_category": "ANDA", "marketing_start_date": "20210810", "listing_expiration_date": "20261231"}