Lisinopril Pharmaceutical Reference Standards

Aligns Pharma science supply high-quality impurities reference standards of Lisinopril, pharmacopeial and non-pharmacopeial Lisinopril impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Lisinopril impurities reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown impurities and the assessment of genotoxic potential.

Lisinopril is a dihydrate salt of Lisinopril which is a potent ACE inhibitor which shows cardiotonic and antihypertensive effects.

Our Lisinopril impurities reference standard offering includes

• Lisinopril related products are thoroughly characterized with NMR, MASS, IR and HPLC/ GC purity.
• Lisinopril products are supplied with detailed COA & analytical data meeting regulatory compliance.
• We can also provide Lisinopril EP/USP traceable standards based on your requirements.
• The supplied Lisinopril related products are re-tested at regular intervals.