Class III ยท Low risk
Lidocaine Patch 5%
Labeling: Typographical error on the upper left-hand side of the box and individual patch label that has the incorrect dosage form stating, each tablet contains instead of each adhesive patch contains.
National Drug Code
Is NDC 63629-8755-20 recalled?
Lidocaine
Yes — this exact package was recalled
1 FDA recall names the code 63629-8755-20 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.
1 of these recalls is still ongoing.
- Active ingredient
- Lidocaine
- Strength
- LIDOCAINE 50 mg/g
- Form
- Patch · Topical
- Labeler
- Bryant Ranch Prepack
- Type
- Human Prescription Drug
- Product code
- 63629-8755
Recalls naming this package
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
- 63629-1064 Spironolactone 1
- 63629-1067 Spironolactone 1
- 63629-1088 Morphine sulfate 1
- 63629-1089 Morphine sulfate 1
- 63629-3324 Venlafaxine 1
- 63629-6905 See recall 1
Free recall alerts
Know the day your medication is recalled
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