This impurity is related to Fenbendazole 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.
Fenbendazole EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:Methyl (1H-benzimidazol-2-yl)carbamateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Fenbendazole Molecular Formula: C9H9N3O2
Molecular Weight: 191.2
Storage: Store in a cool, dry place.