NDC 0143-9830 – Methotrexate

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

Human Prescription Drug

Product NDC0143-9830

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intra-arterial, Intramuscular, Intrathecal, Intravenous
Marketing category
ANDA · ANDA040632
Marketed since
September 6, 2005
Listing expires
December 31, 2027
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Methotrexate →

Package NDC codes (1)

Package NDCDescriptionSince
0143-9830-011 VIAL in 1 BOX (0143-9830-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIALApr 25, 2017

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