bumetanide

Generic: bumetanide

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler cardinal health 107, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide 1 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-4345
Product ID 55154-4345_c4f8101f-4729-4d40-856e-11555bc93582
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209724
Listing Expiration 2026-12-31
Marketing Start 2019-04-23

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 551544345
Hyphenated Format 55154-4345

Supplemental Identifiers

RxCUI
197418
UPC
0055154434508
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 ANDA209724 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-4345-0) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

bumetanide (1 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c4f8101f-4729-4d40-856e-11555bc93582", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0055154434508"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418"], "spl_set_id": ["0a5577f5-d2fe-4b0d-8245-78ee77df30fd"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-4345-0)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "55154-4345-0", "marketing_start_date": "20190423"}], "brand_name": "Bumetanide", "product_id": "55154-4345_c4f8101f-4729-4d40-856e-11555bc93582", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "55154-4345", "generic_name": "Bumetanide", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA209724", "marketing_category": "ANDA", "marketing_start_date": "20190423", "listing_expiration_date": "20261231"}