Eli Lilly and Company Has Recalled Strattera Capsules

(SafetyAlerts) - The Food and Drug Administration (FDA) has released the following information.


PRODUCT
Strattera Capsules (atomoxetine HC1) 40mg, 24 count bottle, Rx only, Adult Sample Pack. Recall # D-188-3.

CODE
6AE95B.

RECALLING FIRM/MANUFACTURER
Eli Lilly and Company, Indianapolis, IN, by fax on January 10, 2003. Firm initiated recall is ongoing.

REASON
Misbranded; bottle label is incorrectly printed as "First use blister".

VOLUME OF PRODUCT IN COMMERCE
89,360 bottles.

DISTRIBUTION
Nationwide.