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Terlipressin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Terlipressin reference materials. Our portfolio includes both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine derivatives (N-NO products). These reference standards play a crucial role in pharmaceutical R&D, aiding in formulation development, ANDA/DMF submissions, quality control, method validation, stability studies, and impurity profiling—including the identification and assessment of potentially genotoxic impurities.
Each Terlipressin-related product is rigorously characterized and delivered with a detailed Certificate of Analysis (COA) and comprehensive analytical data to ensure regulatory compliance. Upon request, we also offer EP/USP traceable standards. To maintain the highest quality standards, all materials are subject to periodic re-testing and continuous quality monitoring.
Terlipressin
Terlipressin Acetate
Terlipressin EP Impurity A
Terlipressin EP Impurity B
Terlipressin EP Impurity C
Terlipressin EP Impurity D
Terlipressin EP Impurity E
Terlipressin EP Impurity F
Terlipressin EP Impurity G
Terlipressin EP Impurity H
Terlipressin EP Impurity I
Terlipressin EP Impurity J
Terlipressin EP Impurity K
Terlipressin EP Impurity L
Terlipressin Dimer Impurity
Terlipressin Parallel Dimer
Terlipressin Antiparallel Dimer
D-Lys(11)-Terlipressin
D-Pro(10)-Terlipressin
D-Tyr(5)-Terlipressin
Lys(Ac)(11)-Terlipressin
Endo-Asn8a-Terlipressin
