| NDC Code | 71288-166-92 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-166-92) / 10 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 71288-166 |
|---|
| 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 |
|---|
| End Marketing Date | 20260828 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA208696 |
|---|
| Manufacturer | Meitheal Pharmaceuticals Inc. |
|---|
| Substance Name | PEMETREXED DISODIUM HEMIPENTAHYDRATE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/10mL |
|---|
| Pharmacy Classes | Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA] |
|---|