Package 50090-7350-0

{"route": ["ORAL"], "spl_id": "b98f9705-fae8-4aeb-b352-c00942032f1a", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197419"], "spl_set_id": ["dfa1f77d-8209-48e9-a6c7-d3b4725a97db"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7350-0)", "package_ndc": "50090-7350-0", "marketing_start_date": "20241016"}], "brand_name": "Bumetanide", "product_id": "50090-7350_b98f9705-fae8-4aeb-b352-c00942032f1a", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "50090-7350", "generic_name": "BUMETANIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA209916", "marketing_category": "ANDA", "marketing_start_date": "20180130", "listing_expiration_date": "20261231"}