Source: Final Program. Conference titles: Annual Meeting & Exposition. Unidade: FCF
Subjects: CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA, ANTI-HISTAMÍNICOS
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SANTORO, Maria Inês Rocha Miritello et al. Development and validation of HPLC methods for quantitative determination of second generation H1 antihistamines in pharmaceuticals. 2013, Anais.. Gaithersburg: AOAC Internacional, 2013. . Acesso em: 06 out. 2024.APA
Santoro, M. I. R. M., Mothe, C. M. A., Silva, C., Kedor-Hackmann, E. R. M., & Singh, A. K. (2013). Development and validation of HPLC methods for quantitative determination of second generation H1 antihistamines in pharmaceuticals. In Final Program. Gaithersburg: AOAC Internacional.NLM
Santoro MIRM, Mothe CMA, Silva C, Kedor-Hackmann ERM, Singh AK. Development and validation of HPLC methods for quantitative determination of second generation H1 antihistamines in pharmaceuticals. Final Program. 2013 ;[citado 2024 out. 06 ]Vancouver
Santoro MIRM, Mothe CMA, Silva C, Kedor-Hackmann ERM, Singh AK. Development and validation of HPLC methods for quantitative determination of second generation H1 antihistamines in pharmaceuticals. Final Program. 2013 ;[citado 2024 out. 06 ]