Labetalol EP Impurity A Hydrochloride

Labetalol EP Impurity A Hydrochloride is chemically Mixture of 4 stereoisomers of 2-hydroxy-5-[(1Ξ)-1-hydroxy-2-[[(2Ξ)-4-phenylbutan-2-yl]amino]ethyl]benzoic acid hydrochloride (as per EP). It is also known as Labetalol 1-Carboxylic Acid ; Labetalol USP Related Compound A. Labetalol EP Impurity A Hydrochloride is supplied with detailed characterization data compliant with regulatory guideline. Labetalol EP Impurity A Hydrochloride 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 Labetalol.

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