Package 72189-382-60

{"route": ["ORAL"], "spl_id": "2c4cd58a-0293-714d-e063-6394a90a5edd", "openfda": {"unii": ["362O9ITL9D", "9N7R477WCK"], "rxcui": ["836395"], "spl_set_id": ["e8a7c995-e473-ca87-e053-2995a90a5b80"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-382-60)", "package_ndc": "72189-382-60", "marketing_start_date": "20220914"}], "brand_name": "Tramadol Hydrochloride and Acetaminophen", "product_id": "72189-382_2c4cd58a-0293-714d-e063-6394a90a5edd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72189-382", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride and Acetaminophen", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "TRAMADOL HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA207152", "marketing_category": "ANDA", "marketing_start_date": "20220914", "listing_expiration_date": "20261231"}