Levothyroxine EP Impurity D

Levothyroxine EP Impurity D is chemically [4-(4-Hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]acetic acid (as per EP). It is also known as Tetraiodothyroacetic Acid (EP) ; T4-Acetic Acid (USP) ; Levothyroxine USB F. Levothyroxine EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Levothyroxine EP Impurity D 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 Levothyroxine.

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.