Class II ยท Moderate risk
Tikosyn (dofetilide)
Failed Tablet/Capsule Specifications: Product being recalled due to the potential presence of cracked or broken capsules.
National Drug Code
Is NDC 0069-5800-60 recalled?
Tikosyn · 60 CAPSULE in 1 BOTTLE (0069-5800-60)
Yes — this exact package was recalled
1 FDA recall names the code 0069-5800-60 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
- dofetilide
- Strength
- DOFETILIDE .125 mg/1
- Form
- Capsule · Oral
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Type
- Human Prescription Drug
- Product code
- 0069-5800
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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