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Data updated: Mar 10, 2026

ASMANEX HFA

MOMETASONE FUROATE
Respiratory Approved 2014-04-25
3
Indications
--
Phase 3 Trials
11
Years on Market

Details

Status
Prescription
First Approved
2014-04-25
Routes
INHALATION
Dosage Forms
AEROSOL, METERED

Companies

Active Ingredient: MOMETASONE FUROATE

ASMANEX HFA Approval History

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What ASMANEX HFA Treats

1 indications

ASMANEX HFA is approved for 1 conditions since its original approval in 2014. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Asthma
Source: FDA Label

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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.

ASMANEX HFA FDA Label Details

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Indications & Usage

FDA Label (PDF)

ASMANEX HFA is a corticosteroid indicated for: Maintenance treatment of asthma as prophylactic therapy in patients 5 years of age and older. Important limitations: Not indicated for the relief of acute bronchospasm. 1.1 Treatment of Asthma ASMANEX ® HFA is indicated for the maintenance treatment of asthma as prophylactic therapy in patients 5 years of age and older. Important Limitations of Use ASMANEX HFA is NOT indicated for the relief of acute bronchospasm.

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Data Sources

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