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Fluvastatin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Fluvastatin 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 Fluvastatin-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.
Fluvastatin
Fluvastatin Sodium
Fluvastatin EP Impurity A
Fluvastatin EP Impurity A Sodium salt
Fluvastatin EP Impurity B
Fluvastatin USP Related Compound B
Fluvastatin EP Impurity C
Fluvastatin Sodium EP Impurity C
Fluvastatin EP Impurity D
Fluvastatin Sodium EP Impurity D
Fluvastatin EP Impurity E
Fluvastatin EP Impurity F
Fluvastatin Sodium EP Impurity F
Fluvastatin EP Impurity G
Fluvastatin Anti Isomer
Fluvastatin lactone
Fluvastatin Methyl Ester
(3R,5S)-Fluvastatin Sodium Salt
(3S,5R)-Fluvastatin sodium salt
(3S,5S)-Fluvastatin Sodium Salt
Fluvastatin lactone (racemic mixture)
Fluvastatin Z isomer tert-butyl Ester
Fluvastatin lactone S-Isomer
Fluvastatin Impurity 1
Fluvastatin Impurity 2
Fluvastatin Anti Isomer
3-Keto fluvastatin
Fluvastatin Lactone
Fluvastatin 3-Hydroxy-4,6-diene Sodium Salt
