NDC 81643-9270
Floxuridine
Floxuridine
Floxuridine is a Intra-arterial Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Cerona Therapeutics, Inc.. The primary component is Floxuridine.
| Product ID | 81643-9270_1655283e-30b3-4267-b775-33ed0b6999a9 |
| NDC | 81643-9270 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Floxuridine |
| Generic Name | Floxuridine |
| Dosage Form | Injection, Powder, Lyophilized, For Solution |
| Route of Administration | INTRA-ARTERIAL |
| Marketing Start Date | 2022-06-09 |
| Marketing Category | ANDA / |
| Application Number | ANDA075387 |
| Labeler Name | Cerona Therapeutics, Inc. |
| Substance Name | FLOXURIDINE |
| Active Ingredient Strength | 500 mg/1 |
| Pharm Classes | Antimetabolite [EPC], Deoxyuridine [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |