| NDC Code | 81643-9270-1 |
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| Package Description | 1 VIAL in 1 BOX, UNIT-DOSE (81643-9270-1) / 5 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
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| Product NDC | 81643-9270 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Floxuridine |
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| Non-Proprietary Name | Floxuridine |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRA-ARTERIAL |
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| Start Marketing Date | 20220609 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075387 |
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| Manufacturer | JND Therapeutics, Inc. |
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| Substance Name | FLOXURIDINE |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Antimetabolite [EPC], Deoxyuridine [CS] |
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