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.
Pimavanserin
Pimavanserin Acetamide Impurity
Pimavanserin Acid Impurity
Pimavanserin Amine Impurity
Pimavanserin Desfluoro Impurity
Pimavanserin Impurity 10
Pimavanserin Impurity 11
Pimavanserin Impurity 12
Pimavanserin Impurity 13
Pimavanserin Impurity 14
Pimavanserin Impurity 15
Pimavanserin Impurity 16
Pimavanserin Impurity 18
Pimavanserin Impurity 20
Pimavanserin Impurity 21
Pimavanserin Impurity 4
Pimavanserin Impurity 5
Pimavanserin Impurity 6
Pimavanserin Impurity 8
Pimavanserin Impurity 9
Pimavanserin Isobutoxy Amine Impurity
Pimavanserin Isobutoxy Urea Impurity
Pimavanserin Methylallyl Urea Impurity
Pimavanserin Methyle Ester Impurity
Pimavanserin N-Oxide
Pimavanserin Sec-butoxy Urea Impurity
Pimavanserin Tartrate
Pimavanserin Tartrate Impurity F
Pimavanserin Urea Impurity
