Class II ยท Moderate risk
Glimepiride USP
CGMP deviations.
National Drug Code
Is NDC 43063-0587-90 recalled?
Glimepiride · 90 TABLET in 1 BOTTLE, PLASTIC (43063-587-90)
Yes — this exact package was recalled
1 FDA recall names the code 43063-0587-90 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.
- Active ingredient
- Glimepiride
- Strength
- GLIMEPIRIDE 4 mg/1
- Form
- Tablet · Oral
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 43063-0587
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
- 43063-0008 See recall 1
- 43063-0428 See recall 1
- 43063-0509 See recall 1
- 43063-0726 simvastatin 1
- 43063-0727 simvastatin 1
- 43063-0762 Montelukast Sodium 1
Free recall alerts
Know the day your medication is recalled
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