Package 50090-5790-3

{"route": ["ORAL"], "spl_id": "831d953a-7e6c-42ca-a018-41a5a62429dd", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["4a525cf7-2c0c-47c6-aed3-3a395a7120ec"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-5790-1)", "package_ndc": "50090-5790-1", "marketing_start_date": "20220208"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-5790-2)", "package_ndc": "50090-5790-2", "marketing_start_date": "20211008"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-5790-3)", "package_ndc": "50090-5790-3", "marketing_start_date": "20220629"}], "brand_name": "Tramadol Hydrochloride", "product_id": "50090-5790_831d953a-7e6c-42ca-a018-41a5a62429dd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "50090-5790", "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"}