bumetanide

Generic: bumetanide

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide 1 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-119
Product ID 82804-119_6e3d3ea1-830f-4fc6-9c56-b2ec71875dc6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074700
Listing Expiration 2026-12-31
Marketing Start 1996-11-21

Pharmacologic Class

Established (EPC)
loop diuretic [epc]
Physiologic Effect
increased diuresis at loop of henle [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804119
Hyphenated Format 82804-119

Supplemental Identifiers

RxCUI
197418
UPC
0382804119905
UNII
0Y2S3XUQ5H
NUI
N0000175366 N0000175590

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name bumetanide (source: ndc)
Generic Name bumetanide (source: ndc)
Application Number ANDA074700 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (82804-119-90)
source: ndc

Packages (1)

82804-119-90 90 TABLET in 1 BOTTLE (82804-119-90)

Ingredients (1)

bumetanide (1 mg/1)

Linked Drug Pages (1)

Bumetanide ndc-match (0.9)

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"}