Package 82804-119-90
Brand: bumetanide
Generic: bumetanidePackage Facts
Identity
Package NDC
82804-119-90
Digits Only
8280411990
Product NDC
82804-119
Description
90 TABLET in 1 BOTTLE (82804-119-90)
Marketing
Marketing Status
Brand
bumetanide
Generic
bumetanide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6e3d3ea1-830f-4fc6-9c56-b2ec71875dc6", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0382804119905"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418"], "spl_set_id": ["6e3d3ea1-830f-4fc6-9c56-b2ec71875dc6"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-119-90)", "package_ndc": "82804-119-90", "marketing_start_date": "20240708"}], "brand_name": "Bumetanide", "product_id": "82804-119_6e3d3ea1-830f-4fc6-9c56-b2ec71875dc6", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "82804-119", "generic_name": "Bumetanide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA074700", "marketing_category": "ANDA", "marketing_start_date": "19961121", "listing_expiration_date": "20261231"}