Package 50268-774-15

{"route": ["ORAL"], "spl_id": "48365501-3c10-9da0-e063-6394a90a25d3", "openfda": {"unii": ["362O9ITL9D", "9N7R477WCK"], "rxcui": ["836395"], "spl_set_id": ["244f6e5d-e1b4-ba8b-ca6f-af2d8a31d5f0"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-774-15)  / 1 TABLET in 1 BLISTER PACK (50268-774-11)", "package_ndc": "50268-774-15", "marketing_end_date": "20270331", "marketing_start_date": "20150114"}], "brand_name": "Tramadol Hydrochloride and Acetaminophen", "product_id": "50268-774_48365501-3c10-9da0-e063-6394a90a25d3", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "50268-774", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride and Acetaminophen", "labeler_name": "AvPAK", "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": "ANDA090485", "marketing_category": "ANDA", "marketing_end_date": "20270331", "marketing_start_date": "20150114"}