Package 72189-368-60

{"route": ["ORAL"], "spl_id": "3230e687-2f8a-2c27-e063-6294a90a7a1e", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049225"], "spl_set_id": ["e4e27022-581e-ba8c-e053-2a95a90a1ae4"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-368-30)", "package_ndc": "72189-368-30", "marketing_start_date": "20220728"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-368-60)", "package_ndc": "72189-368-60", "marketing_start_date": "20220728"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (72189-368-72)", "package_ndc": "72189-368-72", "marketing_start_date": "20220728"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-368-90)", "package_ndc": "72189-368-90", "marketing_start_date": "20220728"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "72189-368_3230e687-2f8a-2c27-e063-6294a90a7a1e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-368", "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": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20220728", "listing_expiration_date": "20261231"}