August 21, 2002
Forest Pharmaceuticals Has Recalled Levothroid
- The Food and Drug Administration (FDA)
has released the
Levothroid Tablets (levothyroxine sodium tablets, USP),25-mcg.,100-tablet
bottles, Rx Only, NDC #0456-0320-01.Recall # D-385-2.
Lot #120012, Exp. 12/02.
Recalling Firm: Forest Pharmaceuticals, Inc., St. Louis, MO, by letters
dated February 27, 2002.
Manufacturer: Forest Pharmaceuticals, Inc., Cincinnati, OH.
Firm initiated recall is ongoing.
Stability; low potency prior to expiration.
VOLUME OF PRODUCT IN COMMERCE