drugs Class II Updated 2014-04-09

Teva Pharmaceuticals USA recalls Duloxetine Delayed-Release Capsules, USP, 20 mg, Rx Only, 60

Recalled Product

Duloxetine Delayed-Release Capsules, USP, 20 mg, Rx Only, 60 capsules per Bottle, Manufactured in Israel by: Teva Pharmaceutical IND, LTD, Jerusalem, Israel, Manufactured for: Teva Pharmaceuticals USA, Sellersville, PA 18960, NDC 0093-7542-06

Hazard / Issue

Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is voluntarily recalling certain lots of Duloxetine DR Capsules USP, 20 mg, 30 mg & 60 mg due to a customer complaint trend regarding capsule breakage.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 48D001, Exp. 5/2015; 48D002, Exp. 9/2015
View official government recall

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