Drug
Who makes floxuridine?
3 companies list floxuridine as a human prescription drug. Forms: injection, powder, lyophilized, for solution. Routes: intra-arterial.
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 floxuridine
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Fresenius Kabi USA, LLCUnited States | injection, powder, lyophilized, for solution | ANDAANDA075837 | 1 | 6 |
| Hikma Pharmaceuticals USA Inc.United States | injection, powder, lyophilized, for solution | ANDAANDA075387 | 1 | 4 |
| JND Therapeutics, Inc. | injection, powder, lyophilized, for solution | ANDAANDA075387 | 1 | 0 |
Bulk ingredient listings
- Zhejiang ChemPacific Corporation · 1 NDC
Enquiry
Common questions
- Who makes floxuridine?
- 3 companies list floxuridine as a human prescription drug in the openFDA NDC Directory, led by Fresenius Kabi USA, LLC, Hikma Pharmaceuticals USA Inc., JND Therapeutics, Inc.. 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 floxuridine?
- 3 companies list floxuridine under an abbreviated new drug application (ANDA), the application type used for generics. Listing status is from the NDC Directory; it is not a statement of availability.
- Who supplies floxuridine active ingredient?
- 1 company lists floxuridine as a bulk ingredient, including Zhejiang ChemPacific Corporation.