Class II ยท Moderate risk
glyBURIDE MICRONIZED
Labeling: Label Mixup: glyBURIDE MICRONIZED, Tablet, 3 mg may have potentially been mislabeled as the following drug: DIGOXIN, Tablet, 0.125 mg, NDC 00115981101, Pedigree: W003154, EXP: 6/13/2014.
National Drug Code
Is NDC 0093-8035-01 recalled?
Glyburide · 100 TABLET in 1 BOTTLE (0093-8035-01)
Yes — this exact package was recalled
1 FDA recall names the code 0093-8035-01 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
- Glyburide
- Strength
- GLYBURIDE 3 mg/1
- Form
- Tablet
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Drug for Further Processing
- Product code
- 0093-8035
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
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