Tadalafil EP Impurity A & C Mixture - Solicitar cotización

Tadalafil EP Impurity A & C Mixture is chemically (6R,12aS)-6-(Benzo[d][1,3]dioxol-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione compound with (6S,12aR)-6-(benzo[d][1,3]dioxol-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydropyrazino[1',2':1,6]pyrido[3,4-b]indole-1,4-dione (1:1). Tadalafil EP Impurity A & C Mixture is supplied with detailed characterization data compliant with regulatory guideline. Tadalafil EP Impurity A & C Mixture 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 Tadalafil.

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.