NDC 0404-9897
Lidocaine Hydrochloride 20 mg per 1 mL injection, solution
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from AuroMedics Pharma LLC's NDC 55150-165.
Where the pills inside were 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
- Nov 11, 2019 · Class II · AuroMedics Pharma LLC
Presence of Foreign Substance: Foreign material found inside the vial.
Lots: Batch #: CLC190049, Exp 02/2022
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
- Jan 12, 2022
- Package NDCs
0404-9897-05- Official label
- DailyMed (National Library of Medicine), updated Sep 10, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?