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.
Shipping Condition
Ambient
Sample COA Purity
NLT 98%
Inventory Status
Under Development
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Chemical Name: Pravastatin EP Impurity A
Synonym: 6′-Epipravastatin (EP) ; (6R)-Pravastatin Sodium ; Pravastatin USP Related Compound B