This impurity is related to Ceftazidime EP Impurity G Stage-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.
Ceftazidime EP Impurity G Stage-I is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:Tert-butyl (Z)-7-(2-aminothiazol-4-yl)-3-methoxy-10,10-dimethyl-6-oxo-2,9-dioxa-5,8-diazaundec-7-en-11-oateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ceftazidime Molecular Formula: C17H28N4O6S
Molecular Weight: 416.49
Storage: Store in a cool, dry place.