Dr. Reddy's. Receives FDA Approval for ZEMBRACE SymTouch Injection for Acute Treatment of Migraines in Adults

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Dr. Reddy's Laboratories
RDY
announced today that the U.S. Food and Drug Administration (FDA) has approved ZEMBRACE™SymTouch™ (sumatriptan succinate) injection, a drug-device combination product intended for the treatment of acute migraine episodes, with or without aura, in adults who are inadequately managed with existing treatment regimens. ZEMBRACESymTouch is available as a prefilled, ready-to-use, single-dose disposable autoinjector containing 3 mg of sumatriptan, a selective 5-HT1B/ID receptor agonist. The injection is intended to be given subcutaneously.1 "We are pleased to have received FDA approval for ZEMBRACESymTouch," said Raghav Chari, Executive Vice President, Proprietary Products Group at Dr. Reddy's Laboratories. "ZEMBRACESymTouch is the first branded
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