Class III ยท Low risk
CABERGOLINE Tablets
Impurities/Degradation Products: This lot of product will not meet the impurity specification over shelf life
National Drug Code
Is NDC 0093-5420-88 recalled?
Cabergoline · 1 BOTTLE in 1 CARTON (0093-5420-88) / 8 TABLET in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 0093-5420-88 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
- Cabergoline
- Strength
- CABERGOLINE .5 mg/1
- Form
- Tablet · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-5420
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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