| NDC Code | 72485-221-02 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (72485-221-02) > 5.26 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 72485-221 |
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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 |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20200115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210991 |
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| Manufacturer | Armas Pharmaceuticals Inc. |
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| Substance Name | GEMCITABINE HYDROCHLORIDE |
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| Strength | 200 |
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| Strength Unit | mg/5.26mL |
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| Pharmacy Classes | Nucleic Acid Synthesis Inhibitors [MoA], Nucleoside Metabolic Inhibitor [EPC] |
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