Floxuridine - FLOXURIDINE
Navigation: NDC > Supplier starting with: A > APP PHARMACEUTICALS, LLC| Field | Value |
|---|---|
| NDC Code: | 63323-145 |
| Proprietary Name: | Floxuridine |
| Suffix: | |
| Non-Proprietary Name: | FLOXURIDINE |
| Dosage Form: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Method: | INTRA-ARTERIAL |
| Original Marketing Date: | 15-03-2001 |
| Category Name: | ANDA |
| Application Number: | ANDA075837 |
| Labeler: | APP PHARMACEUTICALS, LLC |
| Substance Name: | FLOXURIDINE |
| Active Numerator Strength: | 500 |
| Active Ingredient Unit: | mg/5mL |
| Pharm Classes: | Antimetabolite [EPC],Deoxyuridine [Chemical/Ingredient] |
| DEA Schedule: |