AcelRx Pharmaceuticals submits Zalviso NDA to FDA AcelRx Pharmaceuticals.
AcelRx Pharmaceuticals submits Zalviso NDA to FDA AcelRx Pharmaceuticals, Inc. , a specialty pharmaceutical company focused on the advancement and commercialization of innovative treatments for the treating acute and breakthrough pain, today announced that it submitted a New Drug Software to the U.S here . Zalviso is normally a patient-activated, noninvasive analgesic program, which delivers 15 mcg sufentanil per dose as needed for pain control, subject to a 20 minute lockout period between dosages. The proposed indication for Zalviso is the administration of moderate-to-severe acute pain in adult sufferers in the hospital placing.
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