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 . Braz. J. Pharm. Sci. [Internet]. 2014 Mar. 1 [cited 2024 May 9];50(1):213-2. Available from: https://revistas.usp.br/bjps/article/view/80867