TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

REVATIO

SILDENAFIL CITRATE
Cardiovascular Approved 2005-06-03
7
Indications
--
Phase 3 Trials
1
Priority Reviews
20
Years on Market

Details

Status
Prescription
First Approved
2005-06-03
Routes
INTRAVENOUS, ORAL
Dosage Forms
SOLUTION, FOR SUSPENSION, TABLET

Companies

Active Ingredient: SILDENAFIL CITRATE

REVATIO Approval History

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What REVATIO Treats

1 indications

REVATIO is approved for 1 conditions since its original approval in 2005. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Pulmonary Arterial Hypertension
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.

REVATIO FDA Label Details

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Indications & Usage

FDA Label (PDF)

Adults REVATIO is indicated for the treatment of pulmonary arterial hypertension (PAH) (World Health Organization [WHO] Group I) in adults to improve exercise ability and delay clinical worsening [see Clinical Studies ] . Pediatric Patients (1 to 17 Years Old) REVATIO is indicated in pediatric patients 1 to 17 years old for the treatment of pulmonary arterial hypertension (PAH) (WHO Group I) to improve exercise ability and, in pediatric patients too young to perform standardized exercise testing, pulmonary hemodynamics thought to underlie improvements in exercise [see Clinical Studies ] . Adul...

REVATIO Patents & Exclusivity

Exclusivity: Jan 2030

Exclusivity

M-287 Until Jan 2026
M-287 Until Jan 2026
M-287 Until Jan 2026
ODE-469 Until Jan 2030
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.