NDC 51662-1543
Lidocaine Hci 20 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst 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 |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
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
- Aug 7, 2021
- Package NDCs
51662-1543-151662-1543-251662-1543-3- Official label
- DailyMed (National Library of Medicine), updated Jan 27, 2024
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