| NDC Code | 71288-167-96 |
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-167-96) / 50 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 71288-167 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Proprietary Name | Pemetrexed |
| Non-Proprietary Name | Pemetrexed Disodium |
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Usage | INTRAVENOUS |
| Start Marketing Date | 20220525 |
| Marketing Category Name | ANDA |
| Application Number | ANDA208696 |
| Manufacturer | Meitheal Pharmaceuticals Inc. |
| Substance Name | PEMETREXED DISODIUM HEMIPENTAHYDRATE |
| Strength | 500 |
| Strength Unit | mg/50mL |
| Pharmacy Classes | Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA] |