This impurity is related to Fluvastatin Sodium EP Impurity F 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.
Fluvastatin Sodium EP Impurity F is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(4E,6E)-7-(3-(4-Fluorophenyl)-1-isopropyl-1H-indol-2-yl)-3-hydroxyhepta-4,6-dienoic acid, sodium salt (as per EP);Sodium (4E,6E)-7-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]-3-hydroxyhepta-4,6-dienoate (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Fluvastatin Molecular Formula: C24H24FNO3 : Na
Molecular Weight: 393.5 : 23.0
Storage: Store in a cool, dry place.