BRIEF-AMAG Gets FDA Approval Of Makena Subcutaneous Auto-Injector [Reuters]
AMAG PHARMACEUTICALS (AMAG)
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Source: Reuters
BRIEF-AMAG Gets FDA Approval Of Makena Subcutaneous Auto-Injector | Reuters Reuters Staff 1 Min Read Feb 14 (Reuters) - Amag Pharmaceuticals Inc: * AMAG PHARMACEUTICALS ANNOUNCES FDA APPROVAL OF MAKENA® (HYDROXYPROGESTERONE CAPROATE INJECTION) SUBCUTANEOUS AUTO-INJECTOR TO REDUCE THE RISK OF PRETERM BIRTH IN CERTAIN AT-RISK WOMEN * AMAG PHARMACEUTICALS - EXPECTS TO FILE A NEW DRUG APPLICATION THIS QUARTER FOR A NEW CHEMICAL ENTITY (BREMELANOTIDE) * AMAG PHARMACEUTICALS INC - ?EXPECTS SUBCUTANEOUS AUTO-INJECTOR TO BE AVAILABLE IN SECOND HALF OF MARCH * AMAG PHARMACEUTICALS INC - WILL CONTINUE TO OFFER IM FORMULATION OF MAKENA IN BOTH SINGLE-DOSE AND MULTI-DOSE VIALS * AMAG PHARMACEUTICALS INC - ?MAKEN‘S 7-YEAR ORPHAN DRUG EXCLUSIVITY EXPIRED EARLIER THIS MONTH * AMAG PHARMACEUTICALS - ANNOUNCES FDA APPROVAL OF MAKENA (HYDROXYPROGESTERONE CAPROATE INJECTION) SUBCUTANEOUS AUTO-INJECTOR ?? Source text for Eikon: Further company coverage: All quotes delayed a minimum of 15 minutes. See h
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