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Data / Drug companies / Nafcillin sodium

Nafcillin sodium: 8 companies and 17 products in the FDA NDC directory

Nafcillin sodium is listed in the FDA National Drug Code Directory by 8 companies, with 17 products in commercial distribution. 17 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, powder, for solution; injection, powder, lyophilized, for solution, and the newest product started marketing on February 20, 2026.

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Companies listing it
8
Products
17
Generic (ANDA) products
17 (100.0%)
Application numbers
6
Routes
Intravenous, Intramuscular
Brand names
Nafcillin
openFDA record search
api.fda.gov

Companies that list nafcillin sodium

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Eugia US LLC5injection, powder, for solutionGeneric drugs (ANDA)December 26, 2012
Fresenius Kabi USA, LLC3injection, powder, lyophilized, for solutionGeneric drugs (ANDA)June 30, 2011
Armas Pharmaceuticals Inc.2injection, powder, for solutionGeneric drugs (ANDA)November 1, 2023
Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.2injection, powder, for solutionGeneric drugs (ANDA)January 31, 2025
Onesource Specialty Pharma Limited2injection, powder, for solutionGeneric drugs (ANDA)February 20, 2026
Avenacy, LLC1injection, powder, for solutionGeneric drugs (ANDA)February 1, 2025
NorthStar RxLLC1injection, powder, for solutionGeneric drugs (ANDA)July 1, 2024
Sagent Pharmaceuticals1injection, powder, for solutionGeneric drugs (ANDA)April 15, 2025

Dosage forms

Dosage formProductsShare
Injection, powder, for solution1482.4%
Injection, powder, lyophilized, for solution317.6%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)17100%

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.