NDC 55150-164
Lidocaine Hydrochloride 20 mg per 1 mL injection, solution
On the label: AuroMedics Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Recalls
- May 18, 2026 · Class III · Eugia US LLC
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Lots: Lot, expiry: Lot 3LC26029A, exp Feb-2029; Lot 3LC26031A, exp Mar-2029
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, epidural; infiltration; intracaudal; perineural
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA203082
- On the market since
- Mar 14, 2013
- Package NDCs
55150-164-02- Official label
- DailyMed (National Library of Medicine), updated Feb 11, 2026
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