This impurity is related to Pravastatin EP Impurity G 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.
Pravastatin EP Impurity G is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:Sodium (3R,5R)-3,5-dihydroxy-7-[(1S,2S)-6-hydroxy-2-methyl-1,2-dihydronaphthalen-1-yl] heptanoateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Pravastatin Molecular Formula: C18H23O5 : Na
Molecular Weight: 319.4 : 23.0
Storage: Store in a cool, dry place.