TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

BLUDIGO

INDIGOTINDISULFONATE SODIUM
Approved 2022-07-08
1
Indication
--
Phase 3 Trials
3
Years on Market

Details

Status
Prescription
First Approved
2022-07-08
Routes
INTRAVENOUS
Dosage Forms
SOLUTION

Companies

Active Ingredient: INDIGOTINDISULFONATE SODIUM

BLUDIGO Approval History

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What BLUDIGO Treats

1 FDA approvals

Originally approved for its first indication in 2022 .

  • Other (1)
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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.

BLUDIGO FDA Label Details

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Indications & Usage

FDA Label (PDF)

BLUDIGO is indicated for use as a visualization aid in the cystoscopic assessment of the integrity of the ureters in adults following urological and gynecological open, robotic, or endoscopic surgical procedures. BLUDIGO is a diagnostic dye indicated for use as a visualization aid in the cystoscopic assessment of the integrity of the ureters in adults following urological and gynecological open, robotic, or endoscopic surgical procedures.

BLUDIGO Patents & Exclusivity

Latest Patent: Dec 2037
Exclusivity: Jul 2027

Patents (3 active)

US10927258 Expires Dec 23, 2037
US11499050 Expires Dec 23, 2037
US11845867 Expires Nov 25, 2036

Exclusivity

NCE Until Jul 2027
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.