Metoclopramide EP Impurity A

Novel validated stability-indicating UPLC method for the determination of Metoclopramide and its degradation impurities in API and pharmaceutical dosage form
Prathyusha Sowjanya a, Palani Shanmugasundaram a , Petla Naidu b , Sanjeev Kumar Singamsetty
Journal of Pharmacy Research Volume 6, Issue 7, July 2013, Pages 765-773
 
LC–MS characterization of metoclopramide photolysis products
Aubert Maquillea,∗, Jean-Louis Habib Jiwan
Journal of Photochemistry and Photobiology A: Chemistry 205 (2009) 197–202

Metoclopramide EP Impurity A is chemically 4-(Acetylamino)-5-chloro-N-[2-(diethylamino)ethyl]-2-methoxybenzamide . It is also known as Metoclopramide USP Related Compound A ; Metoclopramide BP Impurity A ; N-Acetyl Metoclopramide. Metoclopramide EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Metoclopramide EP Impurity A can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Metoclopramide.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.