NDC 63323-202

Lidocaine 20 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, LLCGrand Island, NY, United StatesMakes it and tests it Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action

Product details

Generic drug
Lidocaine: every company that makes it
Form
injection, solution, infiltration; perineural
Strength
20 mg per 1 mL
Approval
ANDA ANDA088586
On the market since
May 27, 2010
Package NDCs
63323-202-01 63323-202-02
Official label
DailyMed (National Library of Medicine), updated Mar 26, 2025

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