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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
Final FDA approval for generic version of antiretroviral Zerit capsules...

Biotech center to dish out grants, tax breaks
Six months after the state Legislature approved a $1 billion life sciences investment plan, the money is about to start flowing. The Massachusetts Life Sciences Center - the quasi-public agency that will dole out the $1 billion in incentives - begins accepting funding applications tomorrow.
Biotech center to dish out grants, tax breaks...

FDA Approves Gadofosveset for Vascular Imaging
Epix Pharmaceuticals on Monday announced the U.S. approval of gadofosveset trisodium as a contrast agent for use in adults undergoing magnetic resonance angiography (MRA) for the assessment of aortoiliac occlusive disease.
FDA Approves Gadofosveset for Vascular Imaging...

FDA Panel Debates Merits of Next-Generation Opioid Formulations
An FDA advisory panel on November 13–14 examined clinical evidence for a pair of extended-release, abuse-resistant opioid drug products while trying to weigh the needs of patients against the threat of misuse by others. Remoxy XRT, an oxycodone product, and Embeda, a morphine–naltrexone formulation, were designed to deter abusers
FDA Panel Debates Merits of Next-Generation Opioid Formulations...

Lipid-Control Drug Approved by FDA
FDA this week approved a new fibrate drug designed to reduce serum levels of triglycerides and low-density lipoprotein cholesterol while raising high-density lipoproteins. Abbott Laboratories received marketing approval for fenofibric acid, which will be marketed as TriLipix, according to the Illinois pharmaceutical company. The drug can be used alone
Lipid-Control Drug Approved by FDA...

Allergists Respond To FDA Committee Recommendation On Asthma Medication, Encourage Patients With Questions To Contact Physicians
The nation’s allergists urged a Joint FDA Advisory Committee today to continue to make long-acting beta-2 agonists available for the treatment of moderate-to-severe asthma in appropriate patients. More: continued here
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