| NDC Code | 55390-391-50 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (55390-391-50) > 25 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 55390-391 |
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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 | 20120319 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091365 |
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| Manufacturer | Bedford Laboratories |
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| Substance Name | GEMCITABINE HYDROCHLORIDE |
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| Strength | 40 |
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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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