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.
DL-2-Phenylpropionic Acid
Ethoxy Carbonyl Methyl Ester Impurity
Loxoprofen
Loxoprofen Impurity 1
Loxoprofen Impurity 10
Loxoprofen Impurity 11
Loxoprofen Impurity 12
Loxoprofen Impurity 13
Loxoprofen Impurity 14
Loxoprofen Impurity 15
Loxoprofen Impurity 16
Loxoprofen Impurity 2
Loxoprofen Impurity 3
Loxoprofen Impurity 4
Loxoprofen Impurity 5
Loxoprofen Impurity 6
Loxoprofen Impurity 7
Loxoprofen Impurity 8
Loxoprofen Impurity 9
Loxoprofen Impurity A
Loxoprofen Impurity B
Loxoprofen Impurity D
Loxoprofen L-Methol Ester
Loxoprofen Sodium
Loxoprofen Sodium Dihydrate
