This impurity is related to Cefadroxil EP Impurity A 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.
Cefadroxil EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(R)-2-Amino-2-(4-hydroxyphenyl)acetic acid (as per EP & USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Cefadroxil Molecular Formula: C8H9NO3
Molecular Weight: 167.2
Storage: Store in a cool, dry place.