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.
5-O-Acetyl Gemcitabine
5-O-Acetyl Gemcitabine
Gemcitabine
Gemcitabine 3- benzoate impurity
Gemcitabine 5-Benzoate Impurity
Gemcitabine -Beta uridine
Gemcitabine Dihydrogen Phosphate
Gemcitabine EP Impurity A
Gemcitabine EP Impurity B
Gemcitabine EP Impurity C
Gemcitabine Hydrochloride
Gemcitabine Impurity 1
Gemcitabine Impurity 10
Gemcitabine Impurity 11
Gemcitabine Impurity 12
Gemcitabine Impurity 13
Gemcitabine Impurity 2
Gemcitabine Impurity 3
Gemcitabine Impurity 4
Gemcitabine Impurity 5
Gemcitabine Impurity 6
Gemcitabine Impurity 7
Gemcitabine Impurity 8
Gemcitabine Impurity 9
Gemcitabine Monophosphate
Gemcitabine Specified Impurity 1
Gemcitabine Specified Impurity 2
Gemcitabine Specified Impurity 3
Gemcitabine Triphosphate Tri(triethylamine) Salt
