Class III · Low risk
Ezetimibe and Simvastatin Tablets
Failed Impurities/Degradation Specifications: Out of Specification (OOS) for related substances test for Anhydro Simvastatin at the 06-month time point during long-term stability study.
National Drug Code
Is NDC 68462-0323-90 recalled?
ezetimibe and simvastatin · 90 TABLET in 1 BOTTLE (68462-323-90)
Yes — this exact package was recalled
1 FDA recall names the code 68462-0323-90 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
- ezetimibe and simvastatin
- Strength
- EZETIMIBE 10 mg/1; SIMVASTATIN 40 mg/1
- Form
- Tablet · Oral
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Type
- Human Prescription Drug
- Product code
- 68462-0323
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
- 68462-0164 Carvedilol 5
- 68462-0165 Carvedilol 4
- 68462-0248 See recall 4
- 68462-0357 Potassium Chloride 4
- 68462-0562 Diltiazem Hydrochloride 4
- 68462-0249 See recall 3
Free recall alerts
Know the day your medication is recalled
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