Haloperidol Decanoate EP Impurity A (HCl)

Comparative bioavailability study of two haloperidol decanoate containing products
By van Weringh G; Komen B J; Thieme R E; van der Hoeven R T; Vos T
From Pharmacy world & science : PWS (1994), 16(6), 243-7.
 
Haloperidol decanoate in schizophreniform disorders. Clinical and neuroendocrine aspects
By Meco G; Casacchia M; Attenni M; Iafrate A; Castellana F; Ecari U
From Acta psychiatrica Belgica (1983), 83(1), 57-68

Haloperidol Decanoate EP Impurity A (HCl) is chemically 1-[4-(4-Fluorophenyl)-4-oxobutyl]-4-phenylpiperidin-4-yl decanoate hydrochloride(as per EP &USP); . It is also known as Haloperidol Decanoate USP Related Compound D ; Haloperidol decanoate-dechloro analog. Haloperidol Decanoate EP Impurity A (HCl) is supplied with detailed characterization data compliant with regulatory guideline. Haloperidol Decanoate EP Impurity A (HCl) 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 Haloperidol Decanoate.

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.