March 29, 2002Aventis Pharmaceuticals Allegra Recall
- The Food and Drug Administration (FDA) has released the following
Allegra (fexofenadine hydrochloride) Tablets, 60-mg., 100-ct. bottles
packaged in 24-bottle shipping containers, RX, NDC 0088-
1107-47. The responsible firm on the label is Aventis
Pharmaceuticals Inc., Kansas City, MO.
This recall is being extended to add two additional lot numbers-1038814 and
0138816. Recall # D-038-2.
1038814, Exp. Dec. 26, 2003
1038816, Exp. Dec. 26, 2003
1038818, Exp. Dec. 27, 2003
1039714, Exp. Feb. 6, 2004
1039715, Exp. Feb. 6, 2004.
Aventis Pharmaceuticals, Inc., Kansas City, MO, by letter dated September
27, 2001. Firm initiated recall is complete.
Mis-labeling - Shipping carton bears incorrect NDC Bar code.
VOLUME OF PRODUCT IN COMMERCE