Baclofen EP Impurity A

Baclofen EP Impurity A is chemically (4RS)-4-(4-Chlorophenyl)pyrrolidin-2-one (as per EP & USP). It is also known as Baclofen USP Related Compound A. Baclofen EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Baclofen 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 Baclofen.

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