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.
3’,5’-Dihydrodiol Simvastatin
4α,5-Dihydro Simvastatin
Oxo Simvastatin
Simvastatin 6-Oxo Isomer
Simvastatin Acid Ammonium Salt
Simvastatin Acid Glycerol Ester
Simvastatin Acid Triol Sodium Salt
Simvastatin Anhydro Acid Sodium Salt
Simvastatin beta-Hydroxy Impurity
Simvastatin Dihydro Diol Impurity
Simvastatin EP Impurity A (Calcium Salt)
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 K
Simvastatin EP Impurity M
Simvastatin EP Impurity N
Simvastatin Impurity 1
Simvastatin Impurity 2
Simvastatin Impurity 3
Simvastatin Impurity 4
Simvastatin Methyl Ester
Simvastatin beta-Hydroxy Acid Sodium Salt
Simvastatin hydroxy acid
