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Dofetilide Capsules 500 mcg (0.5mg), 60-count bottle, Rx Only, Manufactured by Sun Pharmaceutical Industries Limited, Survey No. 259/15, Dadra-396 191, (U.T of D & NH), India, Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512. NDC 47335-063-86

Drug Recall

Official source record

Recall number
D-1082-2023
Event ID
92725
Classification
Class III
Status
Terminated
Recalling company
SUN PHARMACEUTICAL INDUSTRIES INC
Reason for recall
Out of Specification result observed in content uniformity testing
Report date
August 16, 2023
Recall initiation date
July 18, 2023
Termination date
February 26, 2024
Distribution pattern
Nationwide in the USA

Drug product identifiers

Manufacturer
Sun Pharmaceutical Industries, Inc.
Brand name
DOFETILIDE
Generic name
DOFETILIDE
Substance name
DOFETILIDE
Product NDCs
47335-061; 47335-062; 47335-063
Package NDCs
47335-061-66; 47335-061-79; 47335-061-86; 47335-062-66; 47335-062-79; 47335-062-86; 47335-063-66; 47335-063-79; 47335-063-86
Route
ORAL

Where this information comes from

View FDA enforcement record -- the specific openFDA drug enforcement record this summary was built from.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for details.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to the FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this medication?

Do not start, stop, or change any medication based on this page. Follow the instructions published by the FDA and the recalling company (see the source links below), and talk to your pharmacist or physician if you have questions about a specific medication.

Where can I find more official information?

The source links below, published by the FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

Public Health Trace republishes official FDA drug recall information -- it is not affiliated with the FDA, does not verify or supplement what the source has published, and does not provide medical advice. Never start, stop, or change a medication based on this page. Always follow the guidance of your pharmacist or physician, and consult the official source links above for the most current information. Read the full medical disclaimer.