Class II · Moderate risk
Tikosyn¿ (dofetilide)
Presence of Foriegn Tablets/Capsules: A single Tikosyn¿ (dofetilide) 250 mcg capsule was discovered in one bottle of Tikosyn¿ (dofetilide) 500 mcg (0.5 mg).
National Drug Code
Is NDC 0069-5820-60 recalled?
Tikosyn · 60 CAPSULE in 1 BOTTLE (0069-5820-60)
Yes — this exact package was recalled
1 FDA recall names the code 0069-5820-60 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 .5 mg/1
- Form
- Capsule · Oral
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Type
- Human Prescription Drug
- Product code
- 0069-5820
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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