| NDC Code | 50742-341-01 |
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| Package Description | 1 VIAL in 1 CARTON (50742-341-01) / 20 mL in 1 VIAL |
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| Product NDC | 50742-341 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pemetrexed |
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| Non-Proprietary Name | Pemetrexed Disodium |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20220524 |
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| End Marketing Date | 20251231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204890 |
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| Manufacturer | Ingenus Pharmaceuticals, LLC |
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| Substance Name | PEMETREXED DISODIUM HEMIPENTAHYDRATE |
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| Strength | 500 |
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| Strength Unit | mg/20mL |
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| Pharmacy Classes | Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA] |
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