Japan’s general trading houses are steadily becoming a force to be reckoned with in the pharmaceutical industry — and not…
BUSINESS
DSP’s US Subsidiary Sunovion Announces FDA Acceptance of NDA Resubmission for Epilepsy Treatment Stedesa
Dainippon Sumitomo Pharma’s US subsidiary Sunovion Pharmaceuticals announced on February 27 (US time) that the US FDA has accepted the company’s new drug application (NDA) resubmission for Stedesa (eslicarbazepine acetate) for use in patients with epilepsy. Sunovion submitted the original…
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