Lisinopril

Lisinopril Impurities & Reference Standards

Used throughout the pharmaceutical sector, Lisinopril is an active pharmaceutical ingredient (API) integral to the formulation of medicines and finished dosage forms. Analytical laboratories rely on Lisinopril and its associated impurity standards for method development, quality control testing, and pharmacopoeial compliance (ICH, USP, BP, EP). Each batch of Lisinopril reference standard is accompanied by a Certificate of Analysis (CoA), HPLC purity data, and spectroscopic (NMR/MS/IR) characterization for use in pharmaceutical laboratories worldwide.