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.
4-Fluoroaniline HCl Cabozantinib Impurity
Cabozantinib - 2-Fluoro impurity
Cabozantinib - 3-Fluoro impurity
Cabozantinib - Acid Impurity
Cabozantinib - B
Cabozantinib - Desfluoro
Cabozantinib - G-Imp 06
Cabozantinib - G-Imp 14
Cabozantinib - G-Imp 15
Cabozantinib - G-Imp 18
Cabozantinib - Hydroxy imprity
Cabozantinib - N-Oxide
Cabozantinib Impurity 10
Cabozantinib Impurity 11
Cabozantinib Impurity 12
Cabozantinib Impurity 13
Cabozantinib Impurity 14
Cabozantinib Impurity 2
Cabozantinib Impurity 3
Cabozantinib Impurity 4
Cabozantinib Impurity 5
Cabozantinib Acid impurity
Cabozantinib base
Cabozantinib Dimer Impurity
Cabozantinib Dimer Impurity 1
Cabozantinib Fumarate
Cabozantinib M-Acid impurity
Cabozantinib Quinol Impurity
Cabozantinib S-Malate
