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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. o con la finalidad de. of a generic bioequivalent FDAC) could be discriminatory because it does. Triumeq (600 mg de abacavir, 50 mg de dolutegravir y 300 mg de lamivudine) es la. Bioequivalence of a Dolutegravir, Abacavir and Lamivudine Fixed-Dose. Principio activo solicitado: lamivudina 300 mg+ abacavir 600 mg (kivexa®). The effect of food and bioequivalence (BE) of a new fixed dose combination tablet. Relative biodisponiblily and bioequivalence trial between two Darifenacin extended release oral. Abacavir- Lamivudina biodisponibiliy trial (ELEA Laboratory.). Comparación de los perfiles de disolución para Abacavir Buffer 4,5:. que establece la FDA (Waiver of In Vivo Bioavailability and Bioequivalence Studies for. 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