This impurity is related to Tadalafil EP Impurity A & C Mixture is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
Tadalafil EP Impurity A & C Mixture is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(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)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Tadalafil Molecular Formula: C22H19N3O4
Molecular Weight: 389.4
Storage: Store in a cool, dry place.