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Valaciclovir EP Impurity L  is chemically ,2′-(Methylenediimino)bis[9-[(2-hydroxyethoxy)methyl]-1,9-dihydro-6H-purin-6-one] ;.
It is also known as Acyclovir N-Methylene Dimer ; 2.
Valaciclovir EP Impurity L  is supplied with detailed characterization data compliant with regulatory guideline. Valaciclovir EP Impurity L  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 Valaciclovir.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.