NDC 0404-9900
Lidocaine Hydrochloride 20 mg per 1 mL jelly
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from International Medication Systems, Ltd.'s NDC 76329-3012.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| International Medication Systems, Ltd. | South El Monte, CA, United States | Makes it and tests it | Serious problems, FDA actionDec 19, 2025 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Lidocaine: every company that makes it
- Form
- jelly, topical
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA086283
- On the market since
- Jan 12, 2022
- Package NDCs
0404-9900-05- Official label
- DailyMed (National Library of Medicine), updated Nov 2, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?