bumetanide

Generic: bumetanide

Labeler: edenbridge pharmaceuticals llc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler edenbridge pharmaceuticals llc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide 2 mg/1

Manufacturer
Edenbridge Pharmaceuticals LLC.

Identifiers & Regulatory

Product NDC 42799-121
Product ID 42799-121_462dc93e-f284-3a48-e063-6394a90a7ce1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018225
Listing Expiration 2026-12-31
Marketing Start 2015-10-15

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 42799121
Hyphenated Format 42799-121

Supplemental Identifiers

RxCUI
197417 197418 197419
UPC
0342799120010 0342799119014 0342799121017
UNII
0Y2S3XUQ5H
NUI
N0000175366 N0000175590

Packaging Origin

Original Packager
true

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 NDA018225 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (42799-121-01)
  • 500 TABLET in 1 BOTTLE (42799-121-02)
source: ndc

Packages (2)

42799-121-01 100 TABLET in 1 BOTTLE (42799-121-01) 42799-121-02 500 TABLET in 1 BOTTLE (42799-121-02)

Ingredients (1)

bumetanide (2 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": "462dc93e-f284-3a48-e063-6394a90a7ce1", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0342799120010", "0342799119014", "0342799121017"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["32c4372e-54ea-4fc8-b9f8-827fa4c8edd3"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42799-121-01)", "package_ndc": "42799-121-01", "marketing_start_date": "20151015"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (42799-121-02)", "package_ndc": "42799-121-02", "marketing_start_date": "20151015"}], "brand_name": "Bumetanide", "product_id": "42799-121_462dc93e-f284-3a48-e063-6394a90a7ce1", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "42799-121", "generic_name": "Bumetanide", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "NDA018225", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20151015", "listing_expiration_date": "20261231"}