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SFDA specifies relevant requirements for health food re-registrationIn order to further improve the re-registration of health food, the State Food and Drug Administration (SFDA) recently issued a notice to specify relevant requirements for: the China-made health food2010/7/30
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LEO Pharma A/S voluntarily recalls sodium fusidate for injection (Fucidin)On July 26, 2010, the State Food and Drug Administration (SFDA) was informed by Invida International Trading (Shanghai) Co., Ltd. (Invida) that LEO Pharmaceutical Products Ltd. A/S (LEO Pharma A/S) en2010/7/30
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FDA accepts for filing Cladribine Tablets NDA for MSEMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, announced today that the U.S. Food and Drug Administration (FDA) has accepted for filing the New Drug Application (NDA) for Cladribine2010/7/29
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FDA approves Tris Pharma's first-time generic of Methylphenidate Hydrochloride Oral SolutionTris Pharma, a specialty pharmaceutical company that develops innovative drug delivery technologies, announced that the US Food and Drug Administration (FDA) has approved a first-time generic of Methy2010/7/29
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AHF denies BMS sales reprepresentatives access to healthcare centersToday AIDS Healthcare Foundation (AHF) announced that it has banned pharmaceutical sales representatives from Bristol-Myers Squibb (BMS) from calling on AHF's medical providers and staff in its sixtee2010/7/28
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Novartis launches new OTC children's liquid acetaminophen productNovartis announces the introduction of Triaminic™ Fever Reducer Pain Reliever, the only branded over-the-counter children's liquid acetaminophen product currently available nationwide in the US.2010/7/28
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FDA approves Perrigo's OTC Cetirizine Cherry SyrupPerrigo Company (Nasdaq: PRGO; TASE) today announced that it has received final approval from the U.S. Food and Drug Administration to manufacture and market over-the-counter (OTC) Cetirizine Cherry S2010/7/27
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Tibotec submits NDA for TMC278 anti-HIV compound to FDATibotec Pharmaceuticals today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for TMC278 (rilpivirine), an investigational non-nucleoside reve2010/7/27
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China Sky One Medical receives SFDA approval for producing Ciclopirox Olamine Vaginal SuppositoriesChina Sky One Medical, Inc. ("China Sky One Medical" or "the Company") (Nasdaq: CSKI), a leading fully integrated pharmaceutical company in the People's Republic of China ("PRC"), today announced that2010/7/26
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First generic version of Lovenox receives FDA approval for DVTThe U.S. Food and Drug Administration today approved the first generic version of Lovenox (enoxaparin sodium injection), an anti-coagulant drug used to prevent deep vein thrombosis (DVT), a potentiall2010/7/26