Drug
Who makes moxifloxacin hydrochloride?
18 companies list moxifloxacin hydrochloride as a human prescription drug, including under the names VIGAMOX. Forms: injection, solution; solution; solution/ drops; tablet, film coated. Routes: intravenous, ophthalmic, oral.
Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology
Companies listing moxifloxacin hydrochloride
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| International Medication Systems, Ltd.United States | tablet, film coated | ANDAANDA202632 | 3 | 3 |
| PD-Rx Pharmaceuticals Inc.United States | tablet, film coated | ANDAANDA202632 | 3 | 1 |
| Bryant Ranch PrepackUnited States | tablet, film coated | ANDAANDA202632 | 2 | 1 |
| RemedyRepack, IncUnited States | tablet, film coated | ANDAANDA202632 | 2 | 1 |
| Fresenius Kabi USA, LLCUnited States | injection, solution | NDANDA205572 | 1 | 6 |
| Pharma Packaging Solutions, LLC dba Tjoapack, LLCUnited States | tablet, film coated | ANDAANDA202632 | 1 | 5 |
| Sandoz Industrial Products S.AAustria | solution/ drops | NDA AUTHORIZED GENERICNDA021598 | 1 | 5 |
| ASCLEMED USA INC. DBA ENOVACHEMUnited States | solution | ANDAANDA212616 | 1 | 1 |
| HP Halden Pharma ASNorway | injection, solution | NDANDA205572 | 1 | 1 |
| RedPharm DrugUnited States | solution/ drops | ANDAANDA209698 | 1 | 1 |
| Rising Pharma Holdings, Inc.United States | tablet, film coated | ANDAANDA202632 | 1 | 1 |
| Solaris Pharma CorporationUnited States | tablet, film coated | ANDAANDA206295 | 1 | 1 |
| Somerset Therapeutics Private LimitedIndia | solution/ drops | ANDAANDA209698 | 1 | 1 |
| AvPAK | tablet, film coated | ANDAANDA202632 | 1 | 0 |
| Harrow Eye, LLC | solution/ drops | NDANDA021598 | 1 | 0 |
| MAJOR Pharmaceuticals Inc. | tablet, film coated | ANDAANDA202632 | 1 | 0 |
| Mylan Institutional Inc. | injection, solution | ANDAANDA205833 | 1 | 0 |
| Upsher-Smith Laboratories, Inc. | solution | ANDAANDA212616 | 1 | 0 |
Bulk ingredient listings
- Professional Compounding Centers of America dba PCCAUnited States · 3 NDC
- Anuh Pharma Ltd.India · 1 NDC
- Aragen Life Sciences LimitedIndia · 1 NDC
- Aurobindo Pharma LimitedIndia · 1 NDC
- CHONGQING HUAPONT SHENGCHEM PHARM. CO., LTD. · 1 NDC
- Dr. Reddy's Laboratories LimitedIndia · 1 NDC
- Hunan Jiudian Pharmaceutical Co.,Ltd. · 1 NDC
- MSN Pharmachem Private LimitedIndia · 1 NDC
- YiChang HEC ChangJiang Pharmaceutical Co., Ltd.China · 1 NDC
Orange Book patents
2 unexpired patents list moxifloxacin hydrochloride as the active ingredient, expiring between May 2029 and May 2029. Application holder: HARROW EYE LLC.
Enquiry
Common questions
- Who makes moxifloxacin hydrochloride?
- 18 companies list moxifloxacin hydrochloride as a human prescription drug in the openFDA NDC Directory, led by International Medication Systems, Ltd., PD-Rx Pharmaceuticals Inc., Bryant Ranch Prepack, RemedyRepack, Inc, Fresenius Kabi USA, LLC. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
- Is there a generic VIGAMOX?
- 14 companies list moxifloxacin hydrochloride under an abbreviated new drug application (ANDA), the application type used for generics, and 3 under an NDA or BLA. Listing status is from the NDC Directory; it is not a statement of availability.
- Who supplies moxifloxacin hydrochloride active ingredient?
- 9 companies list moxifloxacin hydrochloride as a bulk ingredient, including Professional Compounding Centers of America dba PCCA, Anuh Pharma Ltd., Aragen Life Sciences Limited, Aurobindo Pharma Limited.