TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

BAXDELA

DELAFLOXACIN MEGLUMINE
Infectious Disease Approved 2017-06-19
2
Indications
--
Phase 3 Trials
2
Priority Reviews
8
Years on Market

Details

Status
Prescription
First Approved
2017-06-19
Routes
ORAL, INTRAVENOUS
Dosage Forms
TABLET, POWDER

Companies

Active Ingredient: DELAFLOXACIN MEGLUMINE

BAXDELA Approval History

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What BAXDELA Treats

2 indications

BAXDELA is approved for 2 conditions since its original approval in 2017. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Acute Bacterial Skin and Skin Structure Infections
  • Community-Acquired Bacterial Pneumonia
Source: FDA Label

BAXDELA Boxed Warning

SERIOUS ADVERSE REACTIONS INCLUDING TENDINITIS, TENDON RUPTURE, PERIPHERAL NEUROPATHY, CENTRAL NERVOUS SYSTEM EFFECTS and EXACERBATION OF MYASTHENIA GRAVIS Fluoroquinolones have been associated with disabling and potentially irreversible serious adverse reactions that have occurred together (5.1), including: Tendinitis and tendon rupture (5.2) Peripheral neuropathy (5.3) Central nervous system effects (5.4) Discontinue BAXDELA immediately and avoid the use of fluoroquinolones, including BAXDELA,...

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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.

BAXDELA FDA Label Details

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Indications & Usage

FDA Label (PDF)

BAXDELA is a fluoroquinolone antibacterial indicated for the treatment of adults with the following infections caused by designated susceptible bacteria: Acute Bacterial Skin and Skin Structure Infections (ABSSSI) Community-Acquired Bacterial Pneumonia (CABP) To reduce the development of drug-resistant bacteria and maintain the effectiveness of BAXDELA and other antibacterial drugs, BAXDELA should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. 1.1 Acute Bacterial Skin and Skin Structure Infections BAXDELA is indicated in adults for t...

⚠️ BOXED WARNING

WARNING: SERIOUS ADVERSE REACTIONS INCLUDING TENDINITIS, TENDON RUPTURE, PERIPHERAL NEUROPATHY, CENTRAL NERVOUS SYSTEM EFFECTS and EXACERBATION OF MYASTHENIA GRAVIS Fluoroquinolones have been associated with disabling and potentially irreversible serious adverse reactions that have occurred together...

BAXDELA Patents & Exclusivity

Latest Patent: Jun 2034
Exclusivity: Jun 2027

Patents (17 active)

US12036219 Expires Jun 2, 2034
US9493582 Expires Feb 27, 2033
US12138257 Expires May 1, 2032
US7728143 Expires Jun 19, 2031
USRE46617 Expires Dec 28, 2029
US8871938 Expires Sep 23, 2029
US9200088 Expires Mar 13, 2029
US9750822 Expires Mar 13, 2029
US7635773 Expires Mar 13, 2029
US8410077 Expires Mar 13, 2029
+ 7 more patents

Exclusivity

NCE Until Jun 2022
GAIN Until Jun 2027
NCE Until Jun 2022
GAIN Until Jun 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.