Methotrexate 61703-0350
Product NDC
61703-0350- Manufacturer
- Hospira, Inc.
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 27, 2005
- Listing Expires
- December 31, 2026
- Application
- NDA011719
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Methotrexate Sodium | 25 mg/mL |
Drug Class
Folate Analog Metabolic Inhibitor [EPC]Folic Acid Metabolism Inhibitors [MoA]
Packaging Options(1)
5 VIAL, MULTI-DOSE in 1 CARTON (61703-350-38) / 2 mL in 1 VIAL, MULTI-DOSE (61703-350-37)