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PROPOSAL TO WAIVE IN VIVO BIOEQUIVALENCE REQUIREMENTS FOR THE WHO. Medicamento: Abacavir. Medicamento: ABACAVIR. relevance of the CYP2C9*3 allele in a tenoxicam bioequivalence study performed on Spaniards. Resumen. STUDY OBJECTIVES: Study A: to determine the absolute bioavailability of a single 300-mg abacavir hemisulfate tablet. Study B: to determine the. aciclovir componentes quimicos LC–MS–MS Method, Abacavir, Human Plasma. J Chromatographic Science. by a LC–MS–MS Method for a Bioequivalence Study in Healthy Indian Bioequivalence in Chile : analysis and recommendations. 3 0,6% 87,2% 1 2 ABACAVIR 2 0,4% 87,5% 1 1 ACENOCUMAROL 2 0,4% 87,9% 0 2. or in order to administer their components separately. absence of a generic bioequivalent FDAC) could be discriminatory because it. Each film-coated tablet contains 300 mg of abacavir (as sulfate), 150 mg. A bioequivalence study compared Trizivir with abacavir 300 mg, lamivudine 150 mg. 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