Methotrexate 63323-0122

Generic: Methotrexate Sodium

Product NDC

63323-0122

Manufacturer: Fresenius Kabi Usa, Llc
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intra-Arterial, Intramuscular, Intrathecal, And Intravenous
Product Type: Human Prescription Drug
Marketing Start: January 22, 2000
Listing Expires: December 31, 2026
Application: ANDA040266

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Active Ingredients

Ingredient	Strength
Methotrexate Sodium	1 g/1

Drug Class

Folate Analog Metabolic Inhibitor [EPC]Folic Acid Metabolism Inhibitors [MoA]

Packaging Options(1)

63323-0122-50

1 VIAL in 1 CARTON (63323-122-50) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

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