Class II ยท Moderate risk
Glimepiride Tablets
Failed Stability Specifications: Micro Labs is recalling two lots due to out of specification results during stability testing.
National Drug Code
Is NDC 42571-0101-01 recalled?
Glimepiride · 100 TABLET in 1 BOTTLE (42571-101-01)
Yes — this exact package was recalled
1 FDA recall names the code 42571-0101-01 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 2 mg/1
- Form
- Tablet · Oral
- Labeler
- Micro Labs Limited
- Type
- Human Prescription Drug
- Product code
- 42571-0101
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
- 42571-0010 See recall 1
- 42571-0020 See recall 1
- 42571-0040 See recall 1
- 42571-0080 See recall 1
- 42571-0110 See recall 1
- 42571-0147 Dorzolamide Hydrochloride and Timolol Maleate ophthalmic Solution 1
Free recall alerts
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