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.
(R)-Zopiclone
Di-O-benzoyl-D-tartaric Acid
Eszopiclone (S-Zopiclone)
N-Demethyl Eszopiclone HCl
N-Desmethyl Zopiclone HCl
R-Zopiclone D8
S-Zopiclone D8
Zopiclone
Zopiclone D4
Zopiclone D8
Zopiclone D8 N-Oxide
Zopiclone Deschloro Impurity
Zopiclone EP Impurity A
Zopiclone EP Impurity B
Zopiclone EP Impurity C
Zopiclone Impurity 1
Zopiclone Impurity 10
Zopiclone Impurity 11
Zopiclone Impurity 12
Zopiclone Impurity 13
Zopiclone Impurity 14
Zopiclone Impurity 2
Zopiclone Impurity 3
Zopiclone Impurity 4
Zopiclone Impurity 5
Zopiclone Impurity 6
Zopiclone Impurity 7
Zopiclone Impurity 8
Zopiclone Impurity 9
