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You are here: Industry Insights > Injectafer

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Injectafer Receives FDA Approval for Single Dose Option for the Treatment of Adult Patients with Iron Deficiency Anemia drugs
May 24, 2021
Daiichi Sankyo, Inc. and American Regent, Inc., today announced that the U.S. Food and Drug Administration (FDA) has approved a single 1000 mg dose option of Injectafer® for the treatment of iron deficiency anemia (IDA) in adult patients

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