NDC 63323-711

Leucovorin Calcium 500 mg per 50 mL injection, powder, lyophilized, for 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 Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action

Product details

Generic drug
Leucovorin: every company that makes it
Form
injection, powder, lyophilized, for solution, intramuscular; intravenous
Strength
500 mg per 50 mL
Approval
ANDA ANDA040286
On the market since
Sep 18, 2010
Package NDCs
63323-711-00
Official label
DailyMed (National Library of Medicine), updated Mar 3, 2022

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