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Alimta
Alimta - 0002-7623-01 - (Pemetrexed disodium)
Drug Information of Alimta
| Product NDC: | 0002-7623 |
| Proprietary Name: | Alimta |
| Non Proprietary Name: | Pemetrexed disodium |
| Active Ingredient(s): | 500 mg/20mL & nbsp; Pemetrexed disodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alimta
| Product NDC: | 0002-7623 |
| Labeler Name: | Eli Lilly and Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021462 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040213 |
Package Information of Alimta
| Package NDC: | 0002-7623-01 |
| Package Description: | 1 VIAL in 1 CARTON (0002-7623-01) > 20 mL in 1 VIAL |
NDC Information of Alimta
| NDC Code | 0002-7623-01 |
| Proprietary Name | Alimta |
| Package Description | 1 VIAL in 1 CARTON (0002-7623-01) > 20 mL in 1 VIAL |
| Product NDC | 0002-7623 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pemetrexed disodium |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20040213 |
| Marketing Category Name | NDA |
| Labeler Name | Eli Lilly and Company |
| Substance Name | PEMETREXED DISODIUM |
| Strength Number | 500 |
| Strength Unit | mg/20mL |
| Pharmaceutical Classes | Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA] |
