| NDC Code | 47335-153-40 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (47335-153-40) > 5 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 47335-153 |
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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 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 | 20110725 |
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| End Marketing Date | 20180930 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078433 |
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| Manufacturer | Sun Pharma Global FZE |
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| Substance Name | GEMCITABINE HYDROCHLORIDE |
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| Strength | 200 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC] |
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