July 11, 2002
American Pharmaceutical Partners Has Recalled
Methotrexate For Injection
- The Food and Drug Administration (FDA) has released the following
Methotrexate For Injection USP, 1 g, lyophilized, preservative free 1 g
Single Dose Vial, Sterile, Rx only, NDC #63323-122-50. Recall # D-341-2
Lot numbers: 210275-1, 210305-1, 210315-1, 210276-1, 210306-1, 210303-1,
210308-1, 210326-1, 210323-1.
Recalling Firm: American Pharmaceutical Partners, Inc., Melrose Park, IL, by
letter dated June 11, 2002.
Manufacturer: Bigmar Pharmaceuticals, Bargengo, Switzerland.
Firm initiated recall is ongoing.
Misbranding; The product is labeled with the wrong NDC # and has a
VOLUME OF PRODUCT IN COMMERCE