August 8, 2002
National Pharmpak Has Recalled Premarin Tablets
- The FDA has released the following information.
Premarin Tablets (conjugated estrogens tablets, USP), 1.25 mg,
100 tablet bottles, Rx only. NDC 0046-0866-81. Recall # D-358-2.
Lot #9000481D, Exp. 01/05.
Recalling Firm: National Pharmpak Services, Inc., Zanesville, OH, by letter
on June 19, 2002
Manufacturer: Ayerst Laboratories, Inc., Rouses Point, NY.
Firm initiated recall is ongoing.
Failure to meet USP dissolution specifications by manufacturer (Wyeth).
VOLUME OF PRODUCT IN COMMERCE