TheraRadar
Data updated: May 26, 2026

CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER (cefoxitin sodium)

Trial Activity: Stable 3 active trials
Infectious Disease Approved 2006-03-10

CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER is indicated for the treatment of Lower Respiratory Tract Infection; Pneumonia; Lung Abscess; Urinary Tract Infection; Intra-Abdominal Infection; Peritonitis; Intra-Abdominal Abscess; Gynecological Infection; Endometritis; Pelvic Cellulitis.

Source: FDA Label • B BRAUN

Development Insights

The University of Queensland conducting 2 trials (33%)
11 indications explored (Broad Platform)
mycobacterium abscessus pulmonary disease (1 trials)
mycobacterium abscessus infection (1 trials)
non-tuberculous mycobacterial (ntm) infections (1 trials)
1
Indication
--
Phase 3 Trials
20
Years on Market

Details

Status
Prescription
First Approved
2006-03-10
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: CEFOXITIN SODIUM

CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER Approval History

2007
2008
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 2006 to 2019
Jul 2019 SUPPL
Label · Labeling
Jun 2013 SUPPL
Label · Labeling
Dec 2012 SUPPL
Mfg · Manufacturing (CMC)

What CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER Treats

10 indications

CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER is approved for 10 conditions since its original approval in 2006. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Lower Respiratory Tract Infection
  • Pneumonia
  • Lung Abscess
  • Urinary Tract Infection
  • Intra-Abdominal Infection
  • Peritonitis
  • Intra-Abdominal Abscess
  • Gynecological Infection
Source: FDA Label

CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER Competitive Set

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

Drugs Similar to CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER

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CEFOXITIN IN PLASTIC CONTAINER
CEFOXITIN SODIUM
10 shared
SAMSON MEDCL
Shared indications:
CLEOCIN HYDROCHLORIDE
CLINDAMYCIN HYDROCHLORIDE
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Pfizer
Shared indications:
Intra-abdominal InfectionPeritonitisIntra-abdominal Abscess +3 more
CLINDAMYCIN HYDROCHLORIDE
CLINDAMYCIN HYDROCHLORIDE
5 shared
MICRO LABS
Shared indications:
Intra-Abdominal InfectionPeritonitisIntra-Abdominal Abscess +2 more
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Active Pipeline

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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.

CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER FDA Label Details

Indications & Usage

FDA Label (PDF)

CEFOXITIN AND DEXTROSE IN DUPLEX CONTAINER is indicated for the treatment of Lower Respiratory Tract Infection; Pneumonia; Lung Abscess; Urinary Tract Infection; Intra-Abdominal Infection; Peritonitis; Intra-Abdominal Abscess; Gynecological Infection; Endometritis; Pelvic Cellulitis.

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Data Sources

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

How We Calculate These Metrics

Trial Activity Stage

Measures the current development activity pattern based on trial phases, status, and trends. Important: This measures R&D activity, not commercial lifecycle.

Trial statuses: "Active" means recruiting or ongoing. "Completed" means reached planned endpoint. "Terminated" means stopped early—often due to safety, efficacy, or business reasons.

  • Growth: High proportion of early-phase trials (Phase 1/2), active development
  • Expansion: Significant Phase 3 activity, approaching or pursuing approvals
  • Mature: Substantial Phase 4 post-marketing studies
  • Stable: Mixed phase distribution, steady development
  • Declining: Low active trial ratio, reduced R&D investment