NDC 55150-512 – Methotrexate

Methotrexate Sodium 200 mg/8mL · Injection, Solution · Intramuscular, Intrathecal, Intravenous, Subcutaneous

Human Prescription Drug

Product NDC55150-512

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Eugia US LLC
Dosage form
Injection, Solution
Route
Intramuscular, Intrathecal, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA201529
Marketed since
September 11, 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 (2)

Package NDCDescriptionSince
55150-512-011 VIAL, SINGLE-DOSE in 1 CARTON (55150-512-01) / 8 mL in 1 VIAL, SINGLE-DOSESep 11, 2024
55150-512-1010 VIAL, SINGLE-DOSE in 1 CARTON (55150-512-10) / 8 mL in 1 VIAL, SINGLE-DOSESep 11, 2024

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