Class II ยท Moderate risk
Capecitabine tablets USP 500 mg
Failed Dissolution Specifications: low test results at the 18 month time-point
National Drug Code
Is NDC 0093-7474-89 recalled?
Capecitabine · 120 TABLET, FILM COATED in 1 BOTTLE (0093-7474-89)
Yes — this exact package was recalled
1 FDA recall names the code 0093-7474-89 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
- Capecitabine
- Strength
- CAPECITABINE 500 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Type
- Human Prescription Drug
- Product code
- 0093-7474
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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