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.
7S Cefdinir Impurity
7S-Cefdinir (USP)
Cefdinir
Cefdinir (E)-Isomer (USP)
Cefdinir 3-Methyl Impurity (USP)
Cefdinir Decarboxy Open Ring Lactone Impurity
Cefdinir glyoxalic analog
Cefdinir Impurity 1
Cefdinir Impurity 2
Cefdinir Impurity 3
Cefdinir Impurity A
Cefdinir Isoxazole Analog
Cefdinir Isoxazole Analog (USP)
Cefdinir Lactone (USP)
Cefdinir Sulfoxide
Cefdinir thiazine analog
Cefdinir Thiazolylacetyl Glycine Oxime Acetal Impurity (USP)
Cefdinir Thiazolylacetyl Glycine Oxime Impurity (USP)
Cefdinir USP Related Compound A
Cefdinir USP Related Compound A (Na)
Cefdinir USP Related Compound B
N-Acetyl Cefdinir
O-Acetyl Cefdinir
Trytil Cefdinir CFD-I IS
