Class III · Low risk
Glimepiride Tablets
Misprint on tablet
National Drug Code
Is NDC 55111-0320-05 recalled?
Glimepiride · 500 TABLET in 1 BOTTLE (55111-320-05)
Yes — this exact package was recalled
1 FDA recall names the code 55111-0320-05 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.
2 of these recalls are still ongoing.
- Active ingredient
- Glimepiride
- Strength
- GLIMEPIRIDE 1 mg/1
- Form
- Tablet · Oral
- Labeler
- Dr. Reddy's Laboratories Limited
- Type
- Human Prescription Drug
- Product code
- 55111-0320
Recalls naming this package
Class III · Low risk
Glimepiride Tablets
Misprint on tablet
Class II · Moderate risk
GLIMEPIRIDE Tablet
Labeling:Label Mixup; GLIMEPIRIDE, Tablet, 1 mg may be potentially mislabeled as clomiPRAMINE HCl, Capsule, 50 mg, NDC 51672401205, Pedigree: AD73525_4, EXP: 5/30/2014.
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
- 55111-0121 Atorvastatin Calcium 4
- 55111-0123 Atorvastatin Calcium 4
- 55111-0180 Tizanidine 4
- 55111-0136 Zenatane 3
- 55111-0179 Tizanidine 3
- 55111-0533 Divalproex Sodium 3
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