Source: Analytical Letters. Unidade: FCF
Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, FÁRMACOS (DETERMINAÇÃO)
ABNT
GOMES, Fábio Pereira et al. Development and validation of stability indicating HPLC methods for quantitative determination of pravastatin, fluvastatin, atorvastatin and rosuvastatin in pharmaceuticals. Analytical Letters, v. 42, n. 12, p. 1784-1804, 2009Tradução . . Acesso em: 14 nov. 2024.APA
Gomes, F. P., García, P. L., Alves, J. M. P., Singh, A. K., Kedor-Hackmann, E. R. M., & Santoro, M. I. R. M. (2009). Development and validation of stability indicating HPLC methods for quantitative determination of pravastatin, fluvastatin, atorvastatin and rosuvastatin in pharmaceuticals. Analytical Letters, 42( 12), 1784-1804.NLM
Gomes FP, García PL, Alves JMP, Singh AK, Kedor-Hackmann ERM, Santoro MIRM. Development and validation of stability indicating HPLC methods for quantitative determination of pravastatin, fluvastatin, atorvastatin and rosuvastatin in pharmaceuticals. Analytical Letters. 2009 ; 42( 12): 1784-1804.[citado 2024 nov. 14 ]Vancouver
Gomes FP, García PL, Alves JMP, Singh AK, Kedor-Hackmann ERM, Santoro MIRM. Development and validation of stability indicating HPLC methods for quantitative determination of pravastatin, fluvastatin, atorvastatin and rosuvastatin in pharmaceuticals. Analytical Letters. 2009 ; 42( 12): 1784-1804.[citado 2024 nov. 14 ]