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Data / Drug companies / Cefepime

Cefepime: 6 companies and 16 products in the FDA NDC directory

Cefepime is listed in the FDA National Drug Code Directory by 6 companies, with 16 products in commercial distribution. 15 of the products (93.8%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, powder, for solution; injection, solution, and the newest product started marketing on September 1, 2022.

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Companies listing it
6
Products
16
Generic (ANDA) products
15 (93.8%)
Application numbers
4
Routes
Intravenous, Intramuscular
openFDA record search
api.fda.gov

Companies that list cefepime

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Apotex Corp.6injection, powder, for solutionGeneric drugs (ANDA)September 1, 2022
WG Critical Care, LLC4injection, powder, for solutionGeneric drugs (ANDA)March 31, 2021
Fresenius Kabi USA, LLC2injection, powder, for solutionGeneric drugs (ANDA)August 30, 2010
Hospira, Inc.2injection, powder, for solutionGeneric drugs (ANDA)August 24, 2020
Baxter Healthcare Corporation1injection, solutionNew drug applications (NDA)August 5, 2008
Samson Medical Technologies LLC1injection, powder, for solutionGeneric drugs (ANDA)October 1, 2018

Dosage forms

Dosage formProductsShare
Injection, powder, for solution1593.8%
Injection, solution16.2%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1593.8%
New drug applications (NDA)16.2%

Pharmacologic classes

Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.