| NDC Code | 0409-0187-01 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-0187-01) / 50 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 0409-0187 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Gemcitabine |
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| Non-Proprietary Name | Gemcitabine |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20101115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079183 |
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| Manufacturer | Hospira, Inc. |
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| Substance Name | GEMCITABINE HYDROCHLORIDE |
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| Strength | 38 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Nucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC] |
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