Package 72162-2197-5

{"route": ["ORAL"], "spl_id": "16d018df-4755-498d-8fcf-b6b06933588e", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197419"], "spl_set_id": ["f6f12a41-ae6d-4ce6-9bb1-e32679af665f"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2197-1)", "package_ndc": "72162-2197-1", "marketing_start_date": "20231215"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2197-5)", "package_ndc": "72162-2197-5", "marketing_start_date": "20231215"}], "brand_name": "Bumetanide", "product_id": "72162-2197_16d018df-4755-498d-8fcf-b6b06933588e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72162-2197", "generic_name": "Bumetanide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA074700", "marketing_category": "ANDA", "marketing_start_date": "19961121", "listing_expiration_date": "20261231"}