NDC 63323-122 – Methotrexate

Methotrexate Sodium 1 g/1 · Injection, Powder, Lyophilized, For Solution · Intra-arterial, Intramuscular, Intrathecal, Intravenous

Human Prescription Drug

Product NDC63323-122

Product details

Brand name
Methotrexate
Generic name
Methotrexate Sodium
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intra-arterial, Intramuscular, Intrathecal, Intravenous
Marketing category
ANDA · ANDA040266
Marketed since
January 22, 2000
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
63323-122-501 VIAL in 1 CARTON (63323-122-50) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIALJan 22, 2000

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