| NDC Code | 70069-835-01 |
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| Package Description | 1 VIAL in 1 CARTON (70069-835-01) / 20 mL in 1 VIAL |
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| Product NDC | 70069-835 |
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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 | 20250415 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA211899 |
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| Manufacturer | Somerset Therapeutics LLC |
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| Substance Name | PEMETREXED DISODIUM HEPTAHYDRATE |
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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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