| NDC Code | 68001-313-56 |
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| Package Description | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (68001-313-56) |
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| Product NDC | 68001-313 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Azacitidine |
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| Non-Proprietary Name | Azacitidine |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20170701 |
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| End Marketing Date | 20261231 |
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| Marketing Category Name | NDA |
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| Application Number | NDA208216 |
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| Manufacturer | BluePoint Laboratories |
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| Substance Name | AZACITIDINE |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Nucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC] |
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