This impurity is related to Cefuroxime 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.
Cefuroxime EP Impurity F is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(6R,7R)-7-[[(E)-(Furan-2-yl)(methoxyimino)acetyl]amino]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Cefuroxime Molecular Formula: C15H15N3O7S
Molecular Weight: 381.4
Storage: Store in a cool, dry place.