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Data / Drug companies / Moxifloxacin hydrochloride

Moxifloxacin hydrochloride: 20 companies and 26 products in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Moxifloxacin hydrochloride is listed in the FDA National Drug Code Directory by 20 companies, with 26 products in commercial distribution. 22 of the products (84.6%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; solution/ drops; injection, solution, and the newest product started marketing on December 12, 2025.

The request: Get every company that lists moxifloxacin hydrochloride in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.

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Companies listing it
20
Products
26
Generic (ANDA) products
22 (84.6%)
Application numbers
7
Routes
Oral, Ophthalmic, Intravenous
Brand names
Moxifloxacin, Moxifloxacin Ophthalmic Solution, Vigamox
openFDA record search
api.fda.gov

Companies that list moxifloxacin hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions3tablet, film coatedGeneric drugs (ANDA)March 4, 2014
PD-Rx Pharmaceuticals, Inc.3tablet, film coatedGeneric drugs (ANDA)March 4, 2014
Bryant Ranch Prepack2tablet, film coatedGeneric drugs (ANDA)March 4, 2014
Remedyrepack Inc.2tablet, film coatedGeneric drugs (ANDA)August 27, 2025
American Health Packaging1tablet, film coatedGeneric drugs (ANDA)March 19, 2014
Asclemed USA, Inc.1solutionGeneric drugs (ANDA)February 10, 2021
Aurobindo Pharma Limited1tablet, film coatedGeneric drugs (ANDA)March 4, 2014
AvPAK1tablet, film coatedGeneric drugs (ANDA)July 22, 2016
Fresenius Kabi USA, LLC1injection, solutionNew drug applications (NDA)March 18, 2015
Harrow Eye, LLC1solution/ dropsNew drug applications (NDA)July 1, 2024
Hp Halden Pharma As1injection, solutionNew drug applications (NDA)August 2, 2017
Kesin Pharma Corporation1tablet, film coatedGeneric drugs (ANDA)December 12, 2025
Major Pharmaceuticals1tablet, film coatedGeneric drugs (ANDA)March 8, 2024
Mylan Institutional LLC1injection, solutionGeneric drugs (ANDA)October 3, 2017
Redpharm Drug1solution/ dropsGeneric drugs (ANDA)November 25, 2024
Rising Pharma Holdings, Inc.1tablet, film coatedGeneric drugs (ANDA)March 4, 2014
Sandoz Inc1solution/ dropsAuthorized generics (NDA)May 7, 2003
Solaris Pharma Corporation1tablet, film coatedGeneric drugs (ANDA)December 12, 2025
Somerset Therapeutics, LLC1solution/ dropsGeneric drugs (ANDA)November 25, 2024
Upsher-Smith Laboratories, LLC1solutionGeneric drugs (ANDA)February 10, 2021

Dosage forms

Dosage formProductsShare
Tablet, film coated1765.4%
Solution/ drops415.4%
Injection, solution311.5%
Solution27.7%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)2284.6%
New drug applications (NDA)311.5%
Authorized generics (NDA)13.8%

Pharmacologic classes

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.