Methotrexate 61703-0350-10

Package NDC

61703-0350-10

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)

61703-0350-38

5 VIAL, MULTI-DOSE in 1 CARTON (61703-350-38) / 2 mL in 1 VIAL, MULTI-DOSE (61703-350-37)

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