Class II · Moderate risk
Lidocaine Patch 5%
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 0591-3525-11 recalled?
Lidocaine
Yes — this exact package was recalled
1 FDA recall names the code 0591-3525-11 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Lidocaine
- Strength
- LIDOCAINE 50 mg/g
- Form
- Patch · Topical
- Labeler
- Actavis Pharma, Inc.
- Type
- Human Prescription Drug
- Product code
- 0591-3525
Recalls naming this package
Class II · Moderate risk
Lidocaine Patch 5%
Labeling: Incorrect or Missing Lot and/or Exp date on the individual transdermal pouches but not in the carton.
Class III · Low risk
Lidocaine Patch 5%
Failed Stability Specifications
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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