This impurity is related to Sodium Fusidate EP Impurity A is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
Sodium Fusidate EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:Ent-(24SR,17Z)-16a-(acetyloxy)-3?11?24,25-tetrahydroxy-4?8,14-trimethyl-18-nor-5?10a-cholest-17(20)-en-21-oic acid (24,25-dihydro-24,25-dihydroxyfusidic acid),Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Fusidic Molecular Formula: C31H50O8
Molecular Weight: 550.7
Storage: Store in a cool, dry place.