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.
Favipiravir Acid Impurity
Favipiravir Chloro Homolog Impurity
Favipiravir Impurity 1
Favipiravir Impurity 10
Favipiravir Impurity 11
Favipiravir Impurity 13
Favipiravir Impurity 14
Favipiravir Impurity 15
Favipiravir Impurity 16
Favipiravir Impurity 17
Favipiravir Impurity 18
Favipiravir Impurity 19
Favipiravir Impurity 2
Favipiravir Impurity 20
Favipiravir Impurity 21
Favipiravir Impurity 22
Favipiravir Impurity 23
Favipiravir Impurity 3
Favipiravir Impurity 4
Favipiravir Impurity 5
Favipiravir Impurity 6
Favipiravir Impurity 7
Favipiravir Impurity 8
Favipiravir Impurity 9
