Duloxetine comes as a delayed-release capsule to take by mouth. It is usually taken once or twice a day with or without food. The capsule should not be chewed or crushed. •Duloxetine is not ...

11 enforcement report. The drug is sold under the brand name Cymbalta. The Duloxetine Delayed-Release Capsules' voluntary recall began on Oct. 10 after the FDA deemed the medication the second-highest ...

The recall affects 7,107 bottles of 500-count, 20 mg Duloxetine Delayed-Release Capsules produced by Towa Pharmaceutical Europe and distributed nationwide. It was initiated on October 10 and has ...

The recall, announced on October 10, affects only 20 mg Duloxetine Delayed-Release Capsules made by Towa Pharmaceutical Europe, targeting over 7,100 bottles with lot number 220128 and an ...

The recall was initiated by Breckenridge Pharmaceutical and covers 7107 bottles of 500-count, 20 mg duloxetine delayed-release capsules. The drug is manufactured by Towa Pharmaceutical Europe and ...

The recall of the Duloxetine Delayed-Release Capsules, produced by Towa Pharmaceutical Europe, was initiated on October 10 and has been given the second highest risk classification by the FDA.

Towa issued the recall for 7,107 bottles, which covers 500-count bottles of 20mg Duloxetine Delayed-Release Capsules, Lot number: 220128, Exp. Date 12/2024, according to the Oct. 11 Class II recall.

Here are three things for consumers to know about the recall. The recall involves 7,101 bottles of duloxetine delayed-release capsules distributed nationwide within the United States, according to the ...

In October 2024, over 7,000 bottles of duloxetine delayed-release capsules were recalled by the manufacturer, over concerns ...

1. How do I know if my medication is impacted by the recall? The recall involves 7,101 bottles of duloxetine delayed-release capsules distributed nationwide within the United States, according to ...