CEFOXITIN SODIUM - Food and Drug Administration

Manufacturer: Food and Drug Administration
Effective date: 2014-05-08
Label type: Indexing - Product Concept
Version: 1
Source: full-release
Hydrated at: 2026-06-05 00:15:00

Label at a glance#

ProductCEFOXITIN SODIUM

Active ingredientCEFOXITIN SODIUM

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

CEFOXITIN SODIUM
CEFOXITIN

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CEFOXITIN SODIUM	Q68050H03T	ACTIM

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Cefoxitin	CEFOXITIN SODIUM	Fresenius Kabi USA, LLC	2a9d1e7b-96ee-4e6c-a1e8-47b76b924422	2023-07-10	Warnings, Adverse reactions	Name fallback generic name: CEFOXITIN SODIUM
Cefoxitin	CEFOXITIN SODIUM	Fresenius Kabi USA, LLC	d02170ff-65aa-48b8-a922-94271c46ffa7	2022-09-23	Warnings, Adverse reactions	Name fallback generic name: CEFOXITIN SODIUM
Cefoxitin and Dextrose	CEFOXITIN SODIUM	B. Braun Medical Inc.	6c7e9485-1ede-411c-8c46-911439332864	2019-07-29	Warnings, Adverse reactions	Name fallback generic name: CEFOXITIN SODIUM

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.