| NDC Code | 57884-4002-1 |
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| Package Description | 1 VIAL in 1 CARTON (57884-4002-1) > 25 mL in 1 VIAL |
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| Product NDC | 57884-4002 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Gemcitabine Hcl |
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| Non-Proprietary Name | Gemcitabine Hydrochloride |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20130508 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202485 |
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| Manufacturer | Jiangsu Hengrui Pharmaceutical Co., Ltd. |
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| Substance Name | GEMCITABINE HYDROCHLORIDE |
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| Strength | 1 |
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| Strength Unit | g/25mL |
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| Pharmacy Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
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