This impurity is related to Tadalafil EP Impurity G 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 G is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(12bR)-6-(1,3-Benzodioxol-5-yl)-12-hydroxy-2-methyl-2,3,6,12b-tetrahydropyrazino[1',2':1,5]pyrrolo[3,4-b]quinoline-1,4-dione Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Tadalafil Molecular Formula: C22H17N3O5
Molecular Weight: 403
Storage: Store in a cool, dry place.