Gabapentin EP Impurity D

Application of UHPLC for determination of Gabapentin drug substance and its related impurities
Ramesha.B1 2 , K. R. Venugopala Reddy 2*, Nischith.H.M 1, Amith Kumar M.K 1, Vinitha.K.V 1 and Vidyanand Ankolekar
Journal of Pharmacy Research 2012,5(8),4437-4442
 
Development and validation of reversed-phase high-performance liquid chromatography method for gabapentin and its related substances in capsule dosage form and excipient compatibility studies
Afroz patan*, alekhya k, vijey aanandhi m
103Asian J Pharm Clin Res, Vol 11, Special Issue 4, 2018, 102-109
 
Determination of gabapentin in bulk drug and in pharmaceutical dosage form by hplc method
B. udaykumar raob, f. maqdoomb and anna pratima nikaljea
J. Chil. Chem. Soc., 54, Nº 4 (2009), págs. 424-427.
 
A Novel Method for Assessing Drug Degradation Product Safety Using Physiologically-Based Pharmacokinetic Models and Stochastic Risk Assessment
Hoa q. nguyen,1 stephen d. stamatis,2 lee e. kirsch1
Nguyen, Stamatis, and Kirsch, journal of pharmaceutical sciences 104:3101–3119, 2015

Gabapentin EP Impurity D is chemically (1-(3-Oxo-2-aza-spiro[4.5]dec-2-ylmethyl)-cyclohexyl)acetic acid. It is also known as Gabapentin USP Related Compound D,. Gabapentin EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Gabapentin EP Impurity D 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 Gabapentin.

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.