JERUSALEM--(BUSINESS WIRE)--Feb. 26, 2006--Teva Pharmaceutical Industries Ltd. (Nasdaq:TEVA) announced today that the U.S. Food and Drug Administration has granted tentative approval for the Company’s ANDAs for Ondansetron Injection USP, 2 mg/mL, packaged in 4 mg/2 mL single-dose vials and Ondansetron Injection USP, 2 mg/mL, packaged in 40 mg/20 mL multiple-dose vials.
