Prempro is subject to another cause for alarm because of a recent recall. This drug recall affects two lots of the product, namely Lot C83323 (exp. 3-10) and Lot D82196 (exp. 12-10). Nearly, 50,000 cartons of Prempro are included in this particular drug recall.
Wyeth Pharmaceuticals, the manufacturer of Prempro, began the drug recall in January of 2010 by way of letter notification. However, people that have moved and have not changed their addresses may not be aware of the recall. The Prempro recall was initiated because the level of estrogen in the affected lots did not meet the specifications outlined in the company’s New Drug Application (NDA).
Prempro is used to treat menopausal symptoms. Wyeth also claimed that the drug improved cardiovascular activity.