NDC 76329-3012

Lidocaine Hydrochloride 20 mg per 1 mL jelly

On the label: International Medication Systems, Ltd..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
International Medication Systems, Ltd.South El Monte, CA, United StatesMakes it and tests it Serious problems, FDA actionDec 19, 2025 · 15 inspections, 1 with FDA action

Product details

Generic drug
Lidocaine: every company that makes it
Form
jelly, topical
Strength
20 mg per 1 mL
Approval
ANDA ANDA086283
On the market since
Aug 7, 1979
Package NDCs
76329-3012-5
Official label
DailyMed (National Library of Medicine), updated Aug 30, 2024

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