This impurity is related to Medroxyprogesterone Acetate EP Impurity I 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.
Medroxyprogesterone Acetate EP Impurity I is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:17a?-hydroxy-6,17a-dimethyl-D-homoandrost-4-ene-3,17-dione Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Progesterone Molecular Formula: C22H32O3
Molecular Weight: 344.5
Storage: Store in a cool, dry place.