NDC 76420-756
Lidocaine Hydrochloride 20 mg per 1 mL injection, solution
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from AuroMedics Pharma LLC's NDC 55150-254.
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 |
| Eugia Steriles Private Limited | Anakapalli, India | Makes it, tests it and packages it | Not inspected on record |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · relabels it
Product details
- Generic drug
- Lidocaine: every company that makes it
- Form
- injection, solution, infiltration; perineural
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA207182
- On the market since
- Oct 30, 2017
- Package NDCs
76420-756-10- Official label
- DailyMed (National Library of Medicine), updated Jun 20, 2024
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