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.
11 α-isomer Mifepristone
11-alpha dioxolane mifepristone
11-ent-Mifepristone
Ethylene-ani-pynyelone of Mifepristone
Hydroxy Mifepristone
Mifepristone
Mifepristone 17-Alpha Isomer
Mifepristone dioxolane impurity
Mifepristone Impirity 12
Mifepristone Impurity 1
Mifepristone Impurity 10
Mifepristone Impurity 11
Mifepristone Impurity 2
Mifepristone Impurity 3
Mifepristone Impurity 4
Mifepristone Impurity 5
Mifepristone Impurity 6
Mifepristone Impurity 7
Mifepristone Impurity 8
Mifepristone Impurity 9
N,N-Dimethylaniline
N-Desmethyl Mifepristone
N-Didesmethyl Mifepristone
