NDC 72189-211
Lidocaine 50 mg per 1 g ointment
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 51672-3008.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharma Canada Inc. | Brampton, Canada | Makes it | No problems foundMar 27, 2026 · 7 inspections |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · relabels it
Recalls
- Aug 31, 2026 · Class II · Sun Pharma /Taro
Failed Content Uniformity Specifications. Out of Specification for Assay during analysis at the 24- month long term stability station, at (25¿C,60%RH).
Lots: Lot # AD48154, Exp: 4/30/2027.
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
- ointment, topical
- Strength
- 50 mg per 1 g
- Approval
- ANDA ANDA086724
- On the market since
- May 7, 2021
- Package NDCs
72189-211-50- Official label
- DailyMed (National Library of Medicine), updated Mar 16, 2026
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