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.
Carbamoyloxy Cefoxitin Acid
Cefoxitin
Cefoxitin Delactam Amide Lactone
Cefoxitin Delactam Lactone
Cefoxitin Dimer Impurity 2
Cefoxitin EP Impurity A
Cefoxitin EP Impurity A Potassium Salt
Cefoxitin EP Impurity A Sodium Salt
Cefoxitin EP Impurity B
Cefoxitin EP Impurity C
Cefoxitin EP Impurity D
Cefoxitin EP Impurity E
Cefoxitin EP Impurity F
Cefoxitin EP Impurity G
Cefoxitin Sodium Salt
Descarbamoyloxy Cefoxitin
Desmethoxy Cefoxitin
Desmethoxy Cefoxitin Sodium Salt
Methoxy Cefoxitin
Methoxy Cefoxitin Potassium Salt
Methoxy Cefoxitin Sodium Salt
