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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Sharma, Nitish, Rao, Surendra Singh, Kumar, Namala Durga Atchuta, Reddy, Pingili Sunil, Reddy, Annarapu Malleswara
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Österreichische Apotheker-Verlagsgesellschaft 2011
Gaiak:
Sarrera elektronikoa: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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