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Data updated: Jun 28, 2026

CEFEPIME IN PLASTIC CONTAINER (cefepime hydrochloride) · Baxter

Infectious Disease Approved 2008-08-05

Cefepime is a fourth-generation cephalosporin antibiotic indicated for the treatment of moderate to severe pneumonia, uncomplicated and complicated urinary tract infections (including pyelonephritis), and uncomplicated skin and skin structure infections. It is also used as empiric monotherapy for febrile neutropenic patients and in combination with metronidazole for the treatment of complicated intra-abdominal infections. To maintain effectiveness and reduce the development of drug-resistant bacteria, cefepime should be used only to treat infections proven or strongly suspected to be caused by susceptible bacteria.

How CEFEPIME IN PLASTIC CONTAINER Works

Cefepime is a bactericidal antibacterial agent that acts by inhibiting bacterial cell wall synthesis. It exerts its effect by binding to specific penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall, which prevents the final transpeptidation step of peptidoglycan synthesis, leading to cell lysis.

1
Indication
--
Phase 3 Trials
17
Years on Market

Details

Status
Prescription
First Approved
2008-08-05
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: CEFEPIME HYDROCHLORIDE

CEFEPIME IN PLASTIC CONTAINER Approval History

2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
14 FDA actions from 2008 to 2025
Jul 2025 SUPPL
Label · Labeling
May 2020 SUPPL
Label · Labeling
May 2016 SUPPL
Label · Labeling

What CEFEPIME IN PLASTIC CONTAINER Treats

5 indications

CEFEPIME IN PLASTIC CONTAINER is approved for 5 conditions since its original approval in 2008. These indications span multiple therapeutic areas including oncology, immunology, and more.

Source: FDA Label

CEFEPIME IN PLASTIC CONTAINER Competitive Set

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Clinical Trial Registry

1 trials
Trial Sponsor ID Phase Status Title
NCT01484015 IRB00015247 NCI-2011-02422, CCCWFU 02110 Ph 1 completed Prolonged or Standard Infusion of Cefepime Hydrochloride in Treating Patients With Febrile Neutropenia
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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.

CEFEPIME IN PLASTIC CONTAINER FDA Label Details

Indications & Usage

FDA Label (PDF)

Cefepime for Injection and Dextrose Injection is a cephalosporin antibacterial indicated in the treatment of the following infections caused by susceptible strains of the designated microorganisms: Pneumonia Empiric therapy for febrile neutropenic patients Uncomplicated and complicated urinary tract infections Uncomplicated skin and skin structure infections Complicated intra-abdominal infections (used in combination with metronidazole) To reduce the development of drug-resistant bacteria and maintain the effectiveness of Cefepime for Injection and Dextrose Injection and other antibacterial dr...

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Data Sources

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