April 2, 2003
IVAX Pharmaceuticals Has Recalled Terazosin
The Food and Drug
Administration (FDA) has released the following information.
Terazosin Hydrochloride Capsules, 1 mg, 500 count bottles, Rx only. Recall #
Lot number 4336-707 Exp. Date Jun 03.
Recalling Firm: IVAX Pharmaceuticals, Miami, FL, by letters on February 11,
Manufacturer: Zenith Goldline Pharmaceuticals, Inc. Firm initiated recall is
Dissolution Failure; 18 month timepoint (stability).
VOLUME OF PRODUCT IN COMMERCE