| NDC Code | 50742-341-01 |
|---|
| Package Description | 1 VIAL in 1 CARTON (50742-341-01) / 20 mL in 1 VIAL |
|---|
| Product NDC | 50742-341 |
|---|
| 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 | 20220524 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204890 |
|---|
| Manufacturer | Ingenus Pharmaceuticals, LLC |
|---|
| Substance Name | PEMETREXED DISODIUM HEMIPENTAHYDRATE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/20mL |
|---|
| Pharmacy Classes | Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA] |
|---|