Class III · Low risk
Dofetilide Capsules 500 mcg
Out of Specification result observed in content uniformity testing
National Drug Code
Is NDC 47335-0063-86 recalled?
Dofetilide · 60 CAPSULE in 1 BOTTLE (47335-063-86)
Yes — this exact package was recalled
2 FDA recalls name the code 47335-0063-86 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
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 47335-0063
Recalls naming this package
Class III · Low risk
Dofetilide Capsules
Failed Content Uniformity Specifications
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
- 47335-0737 Bupropion hydrochloride 6
- 47335-0738 Bupropion hydrochloride 5
- 47335-0506 Cequa 4
- 47335-0343 See recall 2
- 47335-0049 Doxorubicin Hydrochloride 1
- 47335-0154 See recall 1
Free recall alerts
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