Package 53746-617-10

{"route": ["ORAL"], "spl_id": "288548d0-fd1c-4c33-bb0e-f35e47f314aa", "openfda": {"upc": ["0353746617309"], "unii": ["362O9ITL9D", "9N7R477WCK"], "rxcui": ["836395"], "spl_set_id": ["d51600e2-2f73-483c-9b2e-f142bafff16d"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (53746-617-01)", "package_ndc": "53746-617-01", "marketing_start_date": "20091217"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (53746-617-05)", "package_ndc": "53746-617-05", "marketing_start_date": "20091217"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (53746-617-10)", "package_ndc": "53746-617-10", "marketing_start_date": "20091217"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (53746-617-30)", "package_ndc": "53746-617-30", "marketing_start_date": "20091217"}], "brand_name": "Tramadol Hydrochloride and Acetaminophen", "product_id": "53746-617_288548d0-fd1c-4c33-bb0e-f35e47f314aa", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "53746-617", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride and Acetaminophen", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "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_start_date": "20091217", "listing_expiration_date": "20261231"}