bumetanide

Generic: bumetanide

Labeler: solco healthcare llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler solco healthcare llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide 2 mg/1

Manufacturer
Solco Healthcare LLC

Identifiers & Regulatory

Product NDC 43547-898
Product ID 43547-898_4bcc6cdb-3dfa-4757-bac2-a2dc8bd3a9f6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212931
Listing Expiration 2026-12-31
Marketing Start 2025-03-01

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 43547898
Hyphenated Format 43547-898

Supplemental Identifiers

RxCUI
197417 197418 197419
UPC
0343547896102 0343547898106 0343547897109
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 ANDA212931 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (43547-898-10)
  • 500 TABLET in 1 BOTTLE (43547-898-50)
source: ndc

Packages (2)

43547-898-10 100 TABLET in 1 BOTTLE (43547-898-10) 43547-898-50 500 TABLET in 1 BOTTLE (43547-898-50)

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": "4bcc6cdb-3dfa-4757-bac2-a2dc8bd3a9f6", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0343547896102", "0343547898106", "0343547897109"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["4bcc6cdb-3dfa-4757-bac2-a2dc8bd3a9f6"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Solco Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43547-898-10)", "package_ndc": "43547-898-10", "marketing_start_date": "20250301"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (43547-898-50)", "package_ndc": "43547-898-50", "marketing_start_date": "20250301"}], "brand_name": "Bumetanide", "product_id": "43547-898_4bcc6cdb-3dfa-4757-bac2-a2dc8bd3a9f6", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "43547-898", "generic_name": "Bumetanide", "labeler_name": "Solco Healthcare LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA212931", "marketing_category": "ANDA", "marketing_start_date": "20250301", "listing_expiration_date": "20261231"}