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Data updated: Mar 10, 2026

ENBUMYST

BUMETANIDE
Cardiovascular Approved 2025-09-12
1
Indication
--
Phase 3 Trials
0
Years on Market

Details

Status
Prescription
First Approved
2025-09-12
Routes
NASAL
Dosage Forms
SPRAY

Companies

Active Ingredient: BUMETANIDE

ENBUMYST Approval History

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What ENBUMYST Treats

5 indications

ENBUMYST is approved for 5 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Edema
  • Congestive Heart Failure
  • Hepatic Disease
  • Renal Disease
  • Nephrotic Syndrome
Source: FDA Label

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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

ENBUMYST FDA Label Details

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Indications & Usage

ENBUMYST is indicated for the treatment of edema associated with congestive heart failure, hepatic and renal disease, including the nephrotic syndrome in adults. ENBUMYST is a loop diuretic indicated for the treatment of edema associated with congestive heart failure, hepatic and renal disease, including nephrotic syndrome in adults.

ENBUMYST Patents & Exclusivity

Latest Patent: Dec 2040

Patents (3 active)

US12329731 Expires Dec 4, 2040
US11260038 Expires Dec 4, 2040
US11123319 Expires Dec 4, 2040
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.