NDC 0121-0903
Lidocaine Viscous 20 mg per 1 mL solution
On the label: Pharmaceutical Associates, Inc.. It's repackaged: Pharmaceutical Associates, Inc. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-3500.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Repackaging site
- West-Ward Columbus Inc., Columbus, OH, United States · makes it
- PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma, Greenville, SC, United States · repackages it
Product details
- Generic drug
- Lidocaine: every company that makes it
- Form
- solution
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA088802
- On the market since
- Apr 26, 1985
- Package NDCs
0121-0903-150121-0903-40- Official label
- DailyMed (National Library of Medicine), updated Jan 17, 2022
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