Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Grand Island, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action |
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Recalls
- Jul 16, 2026 · Class II · Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in products
Lots: Lot #: 6133801, Exp. Date 01/2028
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Lidocaine: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 20 mg per 1 mL
- Approval
- NDA NDA017584
- On the market since
- Sep 5, 2000
- Package NDCs
63323-208-0163323-208-05- Official label
- DailyMed (National Library of Medicine), updated Feb 20, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?