NDC 61703-161 – Methotrexate

Methotrexate Sodium 25 mg/mL · Injection, Solution · Intramuscular, Intrathecal, Intravenous, Subcutaneous

Human Prescription Drug

Product NDC61703-161

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intramuscular, Intrathecal, Intravenous, Subcutaneous
Marketing category
NDA · NDA011719
Marketed since
November 4, 2024
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
61703-161-055 VIAL, MULTI-DOSE in 1 CARTON (61703-161-05) / 2 mL in 1 VIAL, MULTI-DOSE (61703-161-02)Nov 4, 2024

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