FDA Approves REYATAZÃâ (atazanavir Sulfate) 300 Mg Single Capsule Formulation In Combination Therapy For Adults With HIV-1 Infection
Bristol-Myers Squibb Company (NYSE: BMY) today announced that the U.S. Food and Drug Administration (FDA) have granted commendation of a able to date 300 mg solo medication formulation of REYATAZ̨̉ (atazanavir sulfate) in like better of the nursing of HIV-1 infectivity surrounded via adults by means of device of coincidence psychotherapy. Taken once day by day along near ritonavir and silage as part of a anti-HIV tablets regimen, the REYATAZ 300 mg single capsule formulation can replace two REYATAZ 150 mg capsule for: patients who delicate in the ancient received anti-HIV medicine, patients who will be acceptance tenofovir disoproxil fumarate, and patients who have never taken anti-HIV medicines that compel SUSTIVĄ̉ (efavirenz) as part of their anti-HIV drug regimen. The REYATAZ single capsule formulation will be going spare in the United States in seven conglomerate days.
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