ROXRO Announces FDA Accepts For Review NDA For ROX-888 For The Management Of Acute Moderate To Severe Pain
ROXRO announced that the U.S. Food and Drug Administration (FDA) has accepted for review the New Drug Application (NDA) for its lead investigational prescription drug candidate, ROX-888, for the management of acute moderate to severe pain.
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Tags: accepts, acute, management, moderate, pain, review, roxro, severe
This entry was posted on Saturday, February 7th, 2009 at 11:02 am and is filed under Analgesics Pain Migraine. You can follow any responses to this entry through the RSS 2.0 feed. Both comments and pings are currently closed.



