April 30, 2003
Watson Diagnostics Has Recalled Necon
The Food and Drug
Administration (FDA) released the following information.
Necon 0.5/35 Tablets (norethindrone 0.5mg and ethinyl estradiol 35mcg), 6
tablet dispensers, 28 tablets each, Rx only. Recall # D-185-3.
Lot 50701D00, Exp April 2003.
Watson Diagnostics, Inc, by letter on January 9, 2003. Firm initiated recall
Impurities; product exceeds total impurities specification (stability).
VOLUME OF PRODUCT IN COMMERCE