Title : Development and validation of stability indicating the RP-HPLC method for the estimation of related compounds of guaifenesin in pharmaceutical dosage forms.

Pub. Date : 2011 Oct

PMID : 23781462






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1 MATERIALS AND METHODS: The baseline separation for guaifenesin and all impurities was achieved by utilizing a Water Symmetry C18 (150 mm x 4.6 mm) 5 mum column particle size and a gradient elution method. Water Bardet-Biedl syndrome 9 Homo sapiens