Class II ยท Moderate risk
Glimepiride Tablets
CGMP Deviations: recalling drug products following an FDA inspection.
National Drug Code
Is NDC 68001-0179-00 recalled?
Glimepiride Tablets
Yes — this exact package was recalled
1 FDA recall names the code 68001-0179-00 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.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
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
- 68001-0414 See recall 3
- 68001-0415 See recall 3
- 68001-0581 Haloperidol Decanoate 3
- 68001-0264 See recall 2
- 68001-0313 Azacitidine 2
- 68001-0501 Metoprolol Succinate 2
Free recall alerts
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