Find all the commercial and brand names of generic drug called Duloxetine. This is an invaluable reference resource for healthcare professionals, patients, caregivers and anyone in need of ...

New Jersey-based distributor Rising Pharmaceutical has issued the recall with the compromised products including 30-pill, 90-pilland 1,000-pillbottles of 60 mg duloxetine capsules. The risk level ...

Rising Pharmaceuticals has voluntarily recalled over 233,000 bottles of Duloxetine in the US due ... and 1000-count bottles of 60mg capsules with specific lot numbers and expiration dates.

The capsules of duloxetine were first recalled in November, but the FDA recently categorized the recall as a Class II risk, a situation in which "use of or exposure to a violative product may ...

bottles of duloxetine have been recalled due to potentially containing high levels of cancer-causing impurities.

The recall affected over 233,003 30-count, 90-count and 1,000-count bottles of 60 mg Duloxetine capsules. The FDA does not suggest that patients stop taking Duloxetine immediately but instead talk ...

The recall includes several different formulations of duloxetine delayed-release capsules. The impacted lots cover 20 mg, 30 mg, and 60 mg dosages, across various bottle sizes ranging from 30 to ...

19, various doses of duloxetine delayed-release capsules manufactured by Rising ... Duloxetine—the generic version of drugs sold under the brand names Cymbalta and Irenka—is used to treat ...

The FDA is recalling 30-count, 90-count and 1000-count bottles of duloxetine that contain 60 mg capsules. In total, 233,003 bottles are being recalled. That does not include the 7,107 bottles ...

Patients meeting entry criteria received duloxetine 60 mg once-daily for 12 weeks. Study visits were scheduled after 1, 2, 4, 7, 10 and 12 weeks of treatment. Study drug consisted of 2 capsules ...