NDCFind

Methotrexate 00703-3675-01

Package NDC

00703-3675-01

Product NDC: 00703-3675

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

IngredientStrength
Methotrexate Sodium25 mg/mL

Drug Class

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

Selected Package

00703-3675-01Selected

1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3675-01) / 10 mL in 1 VIAL, SINGLE-DOSE