| NDC Code | 68180-738-01 |
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| Package Description | 1 VIAL in 1 CARTON (68180-738-01) / 20 mL in 1 VIAL |
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| Product NDC | 68180-738 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Decitabine |
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| Non-Proprietary Name | Decitabine |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20191206 |
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| End Marketing Date | 20400101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210756 |
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| Manufacturer | Lupin Pharmaceuticals, Inc. |
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| Substance Name | DECITABINE |
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| Strength | 50 |
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| Strength Unit | mg/20mL |
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| Pharmacy Classes | Nucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC] |
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