Venkatasai is a leading innovator in the field of pharmaceutical reference standards, offering high-quality Reference Standards of Abacavir, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamines (N-NO products). Our Abacavir impurity reference standards play a vital role in pharmaceutical research, supporting product development, ANDA and DMF filings, quality control (QC), method validation, and stability studies. They are also instrumental in identifying unknown impurities and evaluating genotoxic potential. All Abacavir-related products are thoroughly characterized and supplied with comprehensive Certificates of Analysis (COA) and analytical data that comply with regulatory standards. EP/USP traceable standards can also be provided upon request. Furthermore, all supplied products undergo periodic re-testing to ensure continued quality and reliability.
(3R,5S)-Fluvastatin Sodium Salt
(3S,5R)-Fluvastatin sodium salt
(3S,5S)-Fluvastatin Sodium Salt
3-Keto fluvastatin
Fluvastatin
Fluvastatin 3-Hydroxy-4,6-diene Sodium Salt
Fluvastatin Anti Isomer
Fluvastatin Anti Isomer
Fluvastatin EP Impurity A
Fluvastatin EP Impurity A Sodium salt
Fluvastatin EP Impurity B
Fluvastatin EP Impurity C
Fluvastatin EP Impurity D
Fluvastatin EP Impurity E
Fluvastatin EP Impurity F
Fluvastatin EP Impurity G
Fluvastatin Impurity 1
Fluvastatin Impurity 2
Fluvastatin Impurity 3
Fluvastatin Lactone
Fluvastatin lactone
Fluvastatin lactone (racemic mixture)
Fluvastatin lactone S-Isomer
Fluvastatin Methyl Ester
Fluvastatin Sodium EP Impurity C
Fluvastatin Sodium EP Impurity D
Fluvastatin Sodium EP Impurity F
Fluvastatin USP Related Compound B
Fluvastatin Z isomer tert-butyl Ester
Fluvastatin Sodium
