Class II · Moderate risk
Lidocaine Ointment USP
Failed Content Uniformity Specifications. Out of Specification for Assay during analysis at the 24- month long term stability station, at (25¿C,60%RH).
National Drug Code
Is NDC 51672-3008-05 recalled?
Lidocaine · 1 JAR in 1 CARTON (51672-3008-5) / 50 g in 1 JAR
Yes — this exact package was recalled
1 FDA recall names the code 51672-3008-05 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
- Ointment · Topical
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 51672-3008
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
- 51672-1386 Fluocinonide 3
- 51672-1351 Ciclopirox 2
- 51672-1385 Ibuprofen 2
- 51672-2130 Ibuprofen 2
- 51672-3007 Hydrocortisone and Acetic Acid 2
- 51672-4005 Carbamazepine 2
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.