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.
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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.
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| A-S Medication Solutions | 10 | tablet, film coated; solution/ drops | Generic drugs (ANDA) | May 23, 2024 |
| Aurobindo Pharma Limited | 6 | tablet, film coated | Generic drugs (ANDA) | March 27, 2025 |
| PD-Rx Pharmaceuticals, Inc. | 5 | tablet, film coated | Generic drugs (ANDA) | May 23, 2024 |
| Redpharm Drug | 4 | tablet, film coated; solution/ drops | Generic drugs (ANDA) | March 27, 2025 |
| Aurobindo Pharma Limited | 3 | tablet, film coated | Generic drugs (ANDA) | April 26, 2007 |
| Bryant Ranch Prepack | 3 | tablet, film coated | Generic drugs (ANDA) | October 10, 2009 |
| Carlsbad Technology, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | October 10, 2009 |
| Chartwell RX, LLC | 3 | tablet, film coated | Generic drugs (ANDA) | April 13, 2021 |
| Golden State Medical Supply, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | June 9, 2004 |
| Hawaii Repack, Inc. | 3 | tablet, film coated | Generic drugs (ANDA) | April 26, 2007 |
| NuCare Pharmaceuticals,Inc. | 3 | solution/ drops | Authorized generics (NDA) | May 7, 2004 |
| Preferred Pharmaceuticals Inc. | 3 | tablet, film coated; solution/ drops | Generic drugs (ANDA) | July 31, 2026 |
| Proficient Rx LP | 3 | tablet, film coated | Generic drugs (ANDA) | October 10, 2009 |
| Westminster Pharmaceuticals, LLC | 3 | tablet, film coated | Generic drugs (ANDA) | May 23, 2024 |
| American Health Packaging | 2 | tablet, film coated | Generic drugs (ANDA) | May 3, 2026 |
| Aphena Pharma Solutions - Tennessee, LLC | 2 | tablet, film coated | Generic drugs (ANDA) | October 10, 2009 |
| Bayer HealthCare Pharmaceuticals Inc. | 2 | tablet, film coated | New drug applications (NDA) | October 22, 1987 |
| Bryant Ranch Prepack | 2 | tablet, film coated | Generic drugs (ANDA) | October 10, 2009 |
| Remedyrepack Inc. | 2 | tablet, film coated; solution/ drops | Generic drugs (ANDA) | October 15, 2024 |
| Advagen Pharma Ltd | 1 | solution | Generic drugs (ANDA) | March 16, 2022 |
| Advanced Rx of Tennessee, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | March 20, 2025 |
| Altaire Pharmaceuticals Inc. | 1 | solution | Generic drugs (ANDA) | May 4, 2018 |
| Asclemed USA, Inc. | 1 | solution/ drops | Authorized generics (NDA) | May 7, 2004 |
| Bryant Ranch Prepack | 1 | tablet, film coated | Generic drugs (ANDA) | October 10, 2009 |
| Coupler LLC | 1 | tablet, film coated | Generic drugs (ANDA) | August 4, 2026 |
| Direct_Rx | 1 | tablet, film coated | Generic drugs (ANDA) | June 12, 2020 |
| NCS HealthCare of Ky, LLC DBA Vangard Labs | 1 | tablet, film coated | Generic drugs (ANDA) | March 27, 2025 |
| Northwind Health Company, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | March 17, 2023 |
| Northwind Health Company, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | January 21, 2025 |
| PD-Rx Pharmaceuticals, Inc. | 1 | tablet, film coated | Generic drugs (ANDA) | October 10, 2009 |
| Proficient Rx LP | 1 | solution/ drops | Authorized generics (NDA) | May 7, 2004 |
| Proficient Rx LP | 1 | tablet, film coated | Generic drugs (ANDA) | May 23, 2024 |
| Sandoz Inc | 1 | solution/ drops | Authorized generics (NDA) | May 7, 2004 |
| Sandoz Inc | 1 | ointment | New drug applications (NDA) | June 2, 1998 |
| St. Mary's Medical Park Pharmacy | 1 | tablet, film coated | Generic drugs (ANDA) | September 17, 2026 |
| Verityrx, LLC | 1 | tablet, film coated | Generic drugs (ANDA) | May 23, 2024 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Tablet, film coated | 68 | 82.9% |
| Solution/ drops | 11 | 13.4% |
| Solution | 2 | 2.4% |
| Ointment | 1 | 1.2% |
Marketing categories
| Marketing category | Products | Share |
|---|---|---|
| Generic drugs (ANDA) | 68 | 82.9% |
| Authorized generics (NDA) | 11 | 13.4% |
| New drug applications (NDA) | 3 | 3.7% |
Pharmacologic classes
| Class | Products |
|---|---|
| Fluoroquinolone Antibacterial | 75 |
| Quinolone Antimicrobial | 7 |
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.