Application of RP–HPLC method in dissolution testing and statistical evaluation by NASSAM for simultaneous estimation of tertiary combined dosages forms()

A dissolution method with robust high performance liquid chromatographic (HPLC) analysis for immediate release tablet formulation was developed and validated to meet the requirement as per International Conference on Harmonization (ICH) and United States Food and Drug Administration (USFDA) guidelin...

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Detalles Bibliográficos
Autores principales: Upadhyay, Yogesh, Sharma, Nitin, Sarma, G.S., Rawal, Ravindra K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Xi'an Jiaotong University 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762241/
https://www.ncbi.nlm.nih.gov/pubmed/29403944
http://dx.doi.org/10.1016/j.jpha.2014.11.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5762241/
https://www.ncbi.nlm.nih.gov/pubmed/29403944
http://dx.doi.org/10.1016/j.jpha.2014.11.001

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