Famotidine Injection, 20 mg/2 mL
Audience: Pharmacists and other healthcare professionals
Bedford Laboratories and FDA notified healthcare professionals of the voluntary recall of one lot of Famotidine Injection, 20 mg/2 mL (NDC 55390-029-10), Lot# 609336, exp. 04/06, due to a lack of sterility assurance. This prescription product was distributed in August 2004 throughout the United States to wholesalers and distributors, who further distributed the product to hospitals.
[April 29, 2005 - Press Release - Bedford Laboratories, Inc.]