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Data updated: Mar 10, 2026

DIFLUPREDNATE

DIFLUPREDNATE
Dermatology Approved 2021-08-09
8
Indications
--
Phase 3 Trials
4
Years on Market

Details

Status
Prescription
First Approved
2021-08-09
Routes
OPHTHALMIC
Dosage Forms
EMULSION

DIFLUPREDNATE Approval History

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What DIFLUPREDNATE Treats

3 indications

DIFLUPREDNATE is approved for 3 conditions since its original approval in 2021. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Inflammation
  • Pain
  • Uveitis
Source: FDA Label

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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.

DIFLUPREDNATE FDA Label Details

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Indications & Usage

Difluprednate ophthalmic emulsion is a topical corticosteroid that is indicated for: The treatment of inflammation and pain associated with ocular surgery The treatment of endogenous anterior uveitis 1.1 Ocular Surgery Difluprednate ophthalmic emulsion 0.05%, a topical corticosteroid, is indicated for the treatment of inflammation and pain associated with ocular surgery. 1.2 Endogenous Anterior Uveitis Difluprednate ophthalmic emulsion is also indicated for the treatment of endogenous anterior uveitis.

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Data Sources

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