Dr. Reddy’s Laboratories receives USFDA approval for ZEMBRACE SymTouch injection

29 Jan 2016 Evaluate

Dr. Reddy's Laboratories has received the US Food and Drug Administration (FDA) approval for 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. Zembraces ymTouch is available as a prefilled, ready-to-use, single-dose disposable autoinjector containing 3 mg of sumatriptan, a selective 5-HT1 B/ID receptor agonist. The injection is intended to be given subcutaneously. Zembrace Symtouch will be marketed in the United States by Promius Pharma, a wholly-owned specialty company of Dr. Reddy's Laboratories.

Dr. Reddy's Laboratories, is a multinational pharmaceutical company based in Hyderabad, Telangana in India. Dr. Reddy's manufactures and markets a wide range of pharmaceuticals in India and overseas.

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