A Validated Stability-Indicating Liquid-Chromatographic Method for Ranitidine Hydrochloride in Liquid Oral Dosage Form

A selective, specific and stability-indicating gradient reverse phase high-performance liquid chromatographic (HPLC) method was developed for the determination of Ranitidine in presence of its impurities, forced degradation products and placebo substances such as saccharide and parabens. Ultraviolet...

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Autores principales: Sharma, Nitish, Rao, Surendra Singh, Kumar, Namala Durga Atchuta, Reddy, Pingili Sunil, Reddy, Annarapu Malleswara
Formato: Artigo
Lenguaje:Inglês
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2011
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Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3134857/
https://ncbi.nlm.nih.gov/pubmed/21773068
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3797/scipharm.1101-06
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