Validation of analytical methodology for quantification of cefazolin sodium pharmaceutical dosage form by high performance liquid chromatography to be applied for quality control in pharmaceutical industry . Brazilian Journal of Pharmaceutical Sciences, [S. l.], v. 50, n. 1, p. 213–223, 2014. DOI: 10.1590/S1984-82502011000100022. Disponível em: https://revistas.usp.br/bjps/article/view/80867.. Acesso em: 10 may. 2024.