Methotrexate 00703-3678

Product NDC

00703-3678

Manufacturer: Teva Parenteral Medicines, Inc.
Dosage Form: Injection, Solution
Route: Intra-Arterial, Intramuscular, Intrathecal, And Intravenous
Product Type: Human Prescription Drug
Marketing Start: August 1, 2012
Listing Expires: December 31, 2026
Application: ANDA040843

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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)

00703-3678-01

1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3678-01) / 40 mL in 1 VIAL, SINGLE-DOSE

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