Skip to the page

Data / Drug companies / Voriconazole

Voriconazole: 34 companies and 56 products in the FDA NDC directory

Voriconazole is listed in the FDA National Drug Code Directory by 34 companies, with 56 products in commercial distribution. 49 of the products (87.5%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; injection, powder, lyophilized, for solution; powder, for suspension, and the newest product started marketing on August 27, 2026.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
34
Products
56
Generic (ANDA) products
49 (87.5%)
Application numbers
24
Routes
Oral, Intravenous
Brand names
Vfend
openFDA record search
api.fda.gov

Companies that list voriconazole

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Roerig5injection, powder, lyophilized, for solution; tablet, film coatedNew drug applications (NDA)October 24, 2012
American Health Packaging3tablet, film coatedGeneric drugs (ANDA)August 27, 2026
Lupin Pharmaceuticals,Inc.3tablet, film coated; powder, for suspensionGeneric drugs (ANDA)June 1, 2016
Sandoz Inc3tablet, film coated; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 30, 2012
Ajanta Pharma USA Inc.2tablet, film coatedGeneric drugs (ANDA)May 31, 2016
Aurobindo Pharma Limited2tablet, film coatedGeneric drugs (ANDA)January 22, 2016
Camber Pharmaceuticals, Inc.2injection, powder, lyophilized, for solution; powder, for suspensionGeneric drugs (ANDA)August 8, 2025
Major Pharmaceuticals2tablet, film coatedGeneric drugs (ANDA)May 31, 2016
Mylan Institutional Inc.2tablet, film coatedGeneric drugs (ANDA)August 8, 2011
Mylan Pharmaceuticals Inc.2tablet, film coatedGeneric drugs (ANDA)February 15, 2011
NorthStar Rx LLC2tablet, film coatedGeneric drugs (ANDA)January 22, 2016
Safecor Health, LLC2tablet, film coatedGeneric drugs (ANDA)April 6, 2026
Slate Run Pharmaceuticals, LLC2powder, for suspension; injection, powder, lyophilized, for solutionGeneric drugs (ANDA)March 1, 2024
Solco Healthcare US, LLC2tablet, coatedGeneric drugs (ANDA)October 28, 2016
Viona Pharmaceuticals Inc2tablet, film coatedGeneric drugs (ANDA)April 16, 2019
Zydus Lifesciences Limited2tablet, film coatedGeneric drugs (ANDA)May 25, 2016
Amneal Pharmaceuticals LLC1powder, for suspensionGeneric drugs (ANDA)November 29, 2013
AvPAK1tablet, coatedGeneric drugs (ANDA)August 19, 2022
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)May 13, 2025
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)December 12, 2011
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)December 12, 2011
Civica, Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)April 1, 2023
Eugia US LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)February 2, 2023
Fosun Pharma USA Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)January 4, 2021
Fresenius Kabi USA, LLC1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)December 1, 2020
Gland Pharma Limited1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)March 31, 2020
Glenmark Pharmaceuticals Inc., USA1tablet, film coatedGeneric drugs (ANDA)September 4, 2015
Hainan Poly Pharm. Co., Ltd.1injection, solutionGeneric drugs (ANDA)November 20, 2025
Meitheal Pharmaceuticals Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)May 9, 2022
Mylan Pharmaceuticals Inc.1powder, for suspensionAuthorized generics (NDA)December 16, 2013
Novel Laboratories, Inc.1suspensionGeneric drugs (ANDA)June 1, 2016
Ubi Pharma Inc.1injection, powder, lyophilized, for solutionGeneric drugs (ANDA)August 31, 2020
Xellia Pharmaceuticals USA LLC1injection, powder, lyophilized, for solutionNew drug applications (NDA)August 24, 2023
Zhejiang Poly Pharm. Co., Ltd.1powder, for suspensionGeneric drugs (ANDA)April 11, 2025

Dosage forms

Dosage formProductsShare
Tablet, film coated3053.6%
Injection, powder, lyophilized, for solution1425%
Powder, for suspension712.5%
Tablet, coated35.4%
Suspension11.8%
Injection, solution11.8%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)4987.5%
New drug applications (NDA)610.7%
Authorized generics (NDA)11.8%

Pharmacologic classes

ClassProducts
Azole Antifungal56

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.