-
Your RFQ cart is empty!
Simvastatin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Simvastatin 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 Simvastatin-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.
Simvastatin EP Impurity A (Sodium Salt)
Simvastatin EP Impurity B
Simvastatin EP Impurity C
Simvastatin EP Impurity D
Simvastatin EP Impurity E
Simvastatin EP Impurity F
Simvastatin EP Impurity G
Simvastatin EP Impurity H
Simvastatin EP Impurity I
Simvastatin EP Impurity J
Simvastatin EP Impurity M
Simvastatin EP Impurity N
Simvastatin EP Impurity K
Simvastatin 6-Oxo Isomer
Simvastatin Anhydro Acid Sodium Salt
Simvastatin Acid Ammonium Salt
Simvastatin beta-Hydroxy Acid Sodium Salt
Simvastatin Acid Glycerol Ester
Simvastatin Methyl Ester impurity
Simvastatin Acid Triol Sodium Salt
Simvastatin beta-Hydroxy Impurity
Simvastatin Dihydro Diol Impurity
3’,5’-Dihydrodiol Simvastatin
4α,5-Dihydro Simvastatin
Oxo Simvastatin
Simvastatin Impurity 1
Simvastatin Impurity 2
Simvastatin Impurity 3
Simvastatin Impurity 4
Simvastatin hydroxy acid
Simvastatin EP Impurity A (Calcium Salt)
