Methotrexate 00143-9367
Product NDC
00143-9367- Manufacturer
- Hikma Pharmaceuticals Usa Inc.
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intra-Arterial, Intramuscular, Intrathecal, And Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- September 6, 2005
- Listing Expires
- December 31, 2026
- Application
- ANDA040632
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Methotrexate | 1 g/1 |
Drug Class
Folate Analog Metabolic Inhibitor [EPC]Folate Analog Metabolic Inhibitor [EPC]Folic Acid Metabolism Inhibitors [MoA]
Packaging Options(1)
1 VIAL in 1 BOX (0143-9367-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL