NDC 0703-3678 – Methotrexate

Methotrexate Sodium 25 mg/mL · Injection, Solution · Intra-arterial, Intramuscular, Intrathecal, Intravenous

Human Prescription Drug

Product NDC0703-3678

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Teva Parenteral Medicines, Inc.
Dosage form
Injection, Solution
Route
Intra-arterial, Intramuscular, Intrathecal, Intravenous
Marketing category
ANDA · ANDA040843
Marketed since
August 1, 2012
Listing expires
December 31, 2026
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Methotrexate →

Package NDC codes (1)

Package NDCDescriptionSince
0703-3678-011 VIAL, SINGLE-DOSE in 1 CARTON (0703-3678-01) / 40 mL in 1 VIAL, SINGLE-DOSEAug 1, 2012

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