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Tacrolimus
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Tacrolimus 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 Tacrolimus-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.
Tacrolimus Hydrate
Tacrolimus EP Impurity A
Tacrolimus EP Impurity B
Tacrolimus EP Impurity C
Tacrolimus EP Impurity D
Tacrolimus EP Impurity E
Tacrolimus EP Impurity F
Tacrolimus EP Impurity G
Tacrolimus EP Impurity H
Tacrolimus EP Impurity I
Tacrolimus USP Related Compound A
Tacrolimus Regioisomer
Tacrolimus Hydroxy Acid Impurity
Tacrolimus Ring-opening Impurity
Desmethyl Tacrolimus
Tacrolimus 21-Carboxylic acid Impurity
Tacrolimus open ring Impurity
Tacrolimus Dehydro Impurity
Tacrolimus Methyl Acryl Aldehyde Impurity
Tacrolimus Delta Lactone
Tacrolimus Impurity I
Tacrolimus Impurity III
Tacrolimus Impurity IV
Tacrolimus Impurity VII
Tacrolimus Impurity IX
Tacrolimus Impurity X
Tacrolimus Impurity VII
Tacrolimus Impurity XVI
Tacrolimus Impurity VI
Tacrolimus Impurity VII
Tacrolimus Impurity 1
Tacrolimus Impurity 3
Tacrolimus Impurity 4
Tacrolimus Impurity 5
Tacrolimus Impurity 6
Tacrolimus Impurity 7
Tacrolimus Impurity 8
