Package 50090-5789-9

{"route": ["ORAL"], "spl_id": "d2130333-f392-4f3c-b988-c4147c6c9595", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["f9282800-fde7-477a-8b8f-59617ec26f73"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-5789-0)", "package_ndc": "50090-5789-0", "marketing_start_date": "20211008"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-5789-1)", "package_ndc": "50090-5789-1", "marketing_start_date": "20211008"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (50090-5789-2)", "package_ndc": "50090-5789-2", "marketing_start_date": "20211008"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (50090-5789-4)", "package_ndc": "50090-5789-4", "marketing_start_date": "20211008"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-5789-5)", "package_ndc": "50090-5789-5", "marketing_start_date": "20211008"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (50090-5789-9)", "package_ndc": "50090-5789-9", "marketing_start_date": "20211008"}], "brand_name": "Tramadol Hydrochloride", "product_id": "50090-5789_d2130333-f392-4f3c-b988-c4147c6c9595", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "50090-5789", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA211825", "marketing_category": "ANDA", "marketing_start_date": "20190809", "listing_expiration_date": "20271231"}