61703-161Level 3
Methotrexate (Methotrexate)
**Product type:** Human Prescription Drug
**Active ingredient:** METHOTREXATE SODIUM
**Strength:** 25 mg/mL
**Dosage form:** Injection, Solution
**Route:** Intramuscular; Intrathecal; Intravenous; Subcutaneous
**Labeler:** Hospira, Inc.
**Marketing category:** NDA (NDA011719)
**Pharmacologic class:** Folate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]
GET
/api/v1/systems/ndc_fda/nodes/61703-161Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.