| NDC Code | 68001-282-25 |
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| Package Description | 1 VIAL in 1 CARTON (68001-282-25) > 5 mL in 1 VIAL (68001-282-22) |
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| Product NDC | 68001-282 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Gemcitabine Hydrochloride |
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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 | 20210801 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091594 |
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| Manufacturer | BluePoint Laboratories |
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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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