Pravastatin EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Pravastatin EP Impurity A can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Pravastatin.
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Chemical Name: Pravastatin EP Impurity A
Synonym: 6′-Epipravastatin (EP) ; (6R)-Pravastatin Sodium ; Pravastatin USP Related Compound B