bumetanide

Generic: bumetanide

Labeler: advagen pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumetanide
Generic Name bumetanide
Labeler advagen pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide .5 mg/1

Manufacturer
Advagen Pharma Limited

Identifiers & Regulatory

Product NDC 72888-019
Product ID 72888-019_47c8ef6a-8934-2514-e063-6294a90abae6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213942
Listing Expiration 2027-12-31
Marketing Start 2025-01-16

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 72888019
Hyphenated Format 72888-019

Supplemental Identifiers

RxCUI
197417 197418 197419
UPC
0372888021010 0372888020013 0372888019017
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 ANDA213942 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72888-019-01)
source: ndc

Packages (1)

72888-019-01 100 TABLET in 1 BOTTLE (72888-019-01)

Ingredients (1)

bumetanide (.5 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": "47c8ef6a-8934-2514-e063-6294a90abae6", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0372888021010", "0372888020013", "0372888019017"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["94078edd-b9c0-449e-baaf-a9afceccb407"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Advagen Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72888-019-01)", "package_ndc": "72888-019-01", "marketing_start_date": "20250116"}], "brand_name": "Bumetanide", "product_id": "72888-019_47c8ef6a-8934-2514-e063-6294a90abae6", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72888-019", "generic_name": "Bumetanide", "labeler_name": "Advagen Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".5 mg/1"}], "application_number": "ANDA213942", "marketing_category": "ANDA", "marketing_start_date": "20250116", "listing_expiration_date": "20271231"}