Sagent Pharmaceuticals, Inc. Announces the Approval of Zoledronic Acid Injection 4 mg per 100 mL in a Premix Bag

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SCHAUMBURG, Ill., Aug. 5, 2013 (GLOBE NEWSWIRE) -- Sagent Pharmaceuticals, Inc. (Nasdaq:SGNT) today announced the approval of Zoledronic Acid Injection 4 mg per 100 mL, the generic form of the bisphosphonate Zometa®, in a ready-to-use premix IV bag. According to IMS data for the 12 months ending June 2013, the US market for Zoledronic Acid Injection 4 mg approximated $500 million. As with all products in Sagent's portfolio, Zoledronic Acid Injection features Sagent's PreventIV MeasuresSM packaging and labeling, designed to help reduce medication errors.

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