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Final FDA approval for generic version of antiretroviral Zerit capsules
Mylan Inc. has announced that Matrix Laboratories Limited, its India-based subsidiary in which it holds a 71.5% controlling interest, received final approval from the U.S. Food and Drug Administration (FDA) on December 29, for its Abbreviated New Drug Application (ANDA) for Stavudine Capsules USP, 15 mg, 20
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Enhancement of mucosal and cellular immune response in mice by vaccination with respiratory syncytial virus dna encapsulated with transfersome
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Insertion of a targeting peptide on capsid surface loops of human papillomavirus type-16 virus-like particles mediate elimination of anti-dsdna abs-producing b cells with high efficiency.
Page: 36DOI: 10.1097/CJI.0b013e31818dbb8fAuthors: Wang, Huiming *; Yang, Zhao +; Li, Fan ++; He, Yani *; Wang, Shuguang [S]; Yang, Di +; Wu, Yuzhang + (Source: Journal of Immunotherapy)
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The Philadelphia Inquirer on Monday, as part of a continuing series called “Falling Through: Casualties of the Health Insurance Crisis,” examined how more U.S. More: continued here
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Mylan receives FDA approval for Fluoxetine capsules
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NeurogesX Submits NDA For NGX-4010 Dermal Capsaicin Patch For Treatment Of Postherpetic Neuralgia (PHN)
NeurogesX, Inc. (Nasdaq: NGSX), a biopharmaceutical company focused on developing and commercializing novel pain management therapies, announced that it has submitted a new drug application (NDA) with the U.S. Food and Drug Administration (FDA) for approval to market its investigational
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