NDC 63323-123

Methotrexate 25 mg per 1 mL injection, solution

On the label: Fresenius Kabi, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Fresenius Kabi USA, LLCMelrose Park, IL, United StatesMakes it and tests it Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action

Product details

Generic drug
Methotrexate: every company that makes it
Form
injection, solution, intra-arterial; intramuscular; intravenous
Strength
25 mg per 1 mL
Approval
ANDA ANDA040263
On the market since
Sep 10, 2001
Package NDCs
63323-123-10
Official label
DailyMed (National Library of Medicine), updated Mar 24, 2021

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