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www.fdanews.com/articles/96905-the-medicines-company-submits-angiomax-bivalirudin-snda-to-expand-label-to-include-acuity-data

The Medicines Company Submits Angiomax (Bivalirudin) sNDA to Expand Label to Include ACUITY Data

August 7, 2007

The Medicines Company announced it submitted a supplemental new drug application (sNDA) to the U.S. Food and Drug Administration (FDA) for Angiomax (bivalirudin) in support of a proposed new dosage for immediate treatment of patients with acute coronary syndromes (ACS).
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