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.
Barcitinib Lactone Impurity
Baricitinib
Baricitinib Acetic Acid Impurity
Baricitinib Amide Impurity
Baricitinib Diamine Impurity
Baricitinib Impurity 10
Baricitinib Impurity 11
Baricitinib Impurity 12
Baricitinib Impurity 3
Baricitinib Impurity 5
Baricitinib Impurity 6
Baricitinib Impurity 7
Baricitinib Impurity 8
Baricitinib Impurity 9
Baricitinib Impurity A
Baricitinib Impurity B
Baricitinib Impurity C
Baricitinib Impurity III
Baricitinib Impurity IV
Baricitinib Impurity V
Baricitinib Impurity VII
Baricitinib Impurity VIII
Baricitinib Sulfonyl Impurity
