This impurity is related to Prednisolone EP Impurity F 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.
Prednisolone EP Impurity F is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:11a,17,21-Trihydroxypregna-1,4-diene-3,20-dione Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Prednisolone Molecular Formula: C21H28O5
Molecular Weight: 360.4
Storage: Store in a cool, dry place.