July 9, 2003
Meridian Pharmaceuticals Has Recalled
Budesonide BP Micronized
The Food and Drug Administration (FDA) released the following information.
Budesonide BP Micronized, 500mg, 5g, 1g, 25g, 100g bottles, Caution: For
manufacturing, processing and repackaging. Recall # D-274-3.
Lot numbers: 03100205, 03100206, 03100207, 03100208, 03100209, and 03200307.
Meridian Pharmaceuticals, Inc., Decatur, AL, by letters on June 4, 2003.
Firm initiated recall is ongoing.
VOLUME OF PRODUCT IN COMMERCE