NDC Code | 0143-9830-01 |
Package Description | 1 VIAL in 1 BOX (0143-9830-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
Product NDC | 0143-9830 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Methotrexate |
Non-Proprietary Name | Methotrexate |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRA-ARTERIAL; INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS |
Start Marketing Date | 20050906 |
Marketing Category Name | ANDA |
Application Number | ANDA040632 |
Manufacturer | Hikma Pharmaceuticals USA Inc. |
Substance Name | METHOTREXATE |
Strength | 1 |
Strength Unit | g/1 |
Pharmacy Classes | Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA] |