bumex

Generic: bumetanide

Labeler: validus pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name bumex
Generic Name bumetanide
Labeler validus pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

bumetanide .5 mg/1

Manufacturer
Validus Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 30698-630
Product ID 30698-630_3e4799b2-7621-c0b4-e063-6394a90a47b7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018225
Listing Expiration 2026-12-31
Marketing Start 1983-02-28

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 30698630
Hyphenated Format 30698-630

Supplemental Identifiers

RxCUI
197417 197418 197419 205488 205489 205490
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 bumex (source: ndc)
Generic Name bumetanide (source: ndc)
Application Number NDA018225 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (30698-630-01)
source: ndc

Packages (1)

30698-630-01 100 TABLET in 1 BOTTLE (30698-630-01)

Ingredients (1)

bumetanide (.5 mg/1)

Linked Drug Pages (1)

Bumex ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e4799b2-7621-c0b4-e063-6394a90a47b7", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419", "205488", "205489", "205490"], "spl_set_id": ["32dfbea3-eb2b-4070-8605-57ce3e6d5a2f"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Validus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (30698-630-01)", "package_ndc": "30698-630-01", "marketing_start_date": "19830228"}], "brand_name": "Bumex", "product_id": "30698-630_3e4799b2-7621-c0b4-e063-6394a90a47b7", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "30698-630", "generic_name": "Bumetanide", "labeler_name": "Validus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumex", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".5 mg/1"}], "application_number": "NDA018225", "marketing_category": "NDA", "marketing_start_date": "19830228", "listing_expiration_date": "20261231"}