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Data / Drug companies / Ciprofloxacin hydrochloride

Ciprofloxacin hydrochloride: 36 companies and 82 products in the FDA NDC directory

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

Ciprofloxacin hydrochloride is listed in the FDA National Drug Code Directory by 36 companies, with 82 products in commercial distribution. 68 of the products (82.9%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; solution/ drops; solution, and the newest product started marketing on September 17, 2026.

The request: Get every company that lists ciprofloxacin 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
36
Products
82
Generic (ANDA) products
68 (82.9%)
Application numbers
9
Routes
Oral, Ophthalmic
Brand names
Ciprofloxacin, Cipro, Ciprofloxacin HCl Ophthalmic, Ciprofloxacin, Ciloxan
openFDA record search
api.fda.gov

Companies that list ciprofloxacin hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
A-S Medication Solutions10tablet, film coated; solution/ dropsGeneric drugs (ANDA)May 23, 2024
Aurobindo Pharma Limited6tablet, film coatedGeneric drugs (ANDA)March 27, 2025
PD-Rx Pharmaceuticals, Inc.5tablet, film coatedGeneric drugs (ANDA)May 23, 2024
Redpharm Drug4tablet, film coated; solution/ dropsGeneric drugs (ANDA)March 27, 2025
Aurobindo Pharma Limited3tablet, film coatedGeneric drugs (ANDA)April 26, 2007
Bryant Ranch Prepack3tablet, film coatedGeneric drugs (ANDA)October 10, 2009
Carlsbad Technology, Inc.3tablet, film coatedGeneric drugs (ANDA)October 10, 2009
Chartwell RX, LLC3tablet, film coatedGeneric drugs (ANDA)April 13, 2021
Golden State Medical Supply, Inc.3tablet, film coatedGeneric drugs (ANDA)June 9, 2004
Hawaii Repack, Inc.3tablet, film coatedGeneric drugs (ANDA)April 26, 2007
NuCare Pharmaceuticals,Inc.3solution/ dropsAuthorized generics (NDA)May 7, 2004
Preferred Pharmaceuticals Inc.3tablet, film coated; solution/ dropsGeneric drugs (ANDA)July 31, 2026
Proficient Rx LP3tablet, film coatedGeneric drugs (ANDA)October 10, 2009
Westminster Pharmaceuticals, LLC3tablet, film coatedGeneric drugs (ANDA)May 23, 2024
American Health Packaging2tablet, film coatedGeneric drugs (ANDA)May 3, 2026
Aphena Pharma Solutions - Tennessee, LLC2tablet, film coatedGeneric drugs (ANDA)October 10, 2009
Bayer HealthCare Pharmaceuticals Inc.2tablet, film coatedNew drug applications (NDA)October 22, 1987
Bryant Ranch Prepack2tablet, film coatedGeneric drugs (ANDA)October 10, 2009
Remedyrepack Inc.2tablet, film coated; solution/ dropsGeneric drugs (ANDA)October 15, 2024
Advagen Pharma Ltd1solutionGeneric drugs (ANDA)March 16, 2022
Advanced Rx of Tennessee, LLC1tablet, film coatedGeneric drugs (ANDA)March 20, 2025
Altaire Pharmaceuticals Inc.1solutionGeneric drugs (ANDA)May 4, 2018
Asclemed USA, Inc.1solution/ dropsAuthorized generics (NDA)May 7, 2004
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)October 10, 2009
Coupler LLC1tablet, film coatedGeneric drugs (ANDA)August 4, 2026
Direct_Rx1tablet, film coatedGeneric drugs (ANDA)June 12, 2020
NCS HealthCare of Ky, LLC DBA Vangard Labs1tablet, film coatedGeneric drugs (ANDA)March 27, 2025
Northwind Health Company, LLC1tablet, film coatedGeneric drugs (ANDA)March 17, 2023
Northwind Health Company, LLC1tablet, film coatedGeneric drugs (ANDA)January 21, 2025
PD-Rx Pharmaceuticals, Inc.1tablet, film coatedGeneric drugs (ANDA)October 10, 2009
Proficient Rx LP1solution/ dropsAuthorized generics (NDA)May 7, 2004
Proficient Rx LP1tablet, film coatedGeneric drugs (ANDA)May 23, 2024
Sandoz Inc1solution/ dropsAuthorized generics (NDA)May 7, 2004
Sandoz Inc1ointmentNew drug applications (NDA)June 2, 1998
St. Mary's Medical Park Pharmacy1tablet, film coatedGeneric drugs (ANDA)September 17, 2026
Verityrx, LLC1tablet, film coatedGeneric drugs (ANDA)May 23, 2024

Dosage forms

Dosage formProductsShare
Tablet, film coated6882.9%
Solution/ drops1113.4%
Solution22.4%
Ointment11.2%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)6882.9%
Authorized generics (NDA)1113.4%
New drug applications (NDA)33.7%

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.