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Cefadroxil
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Cefadroxil reference materials. Our portfolio includes both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine derivatives (N-NO products). These reference standards play a crucial role in pharmaceutical R&D, aiding in formulation development, ANDA/DMF submissions, quality control, method validation, stability studies, and impurity profiling—including the identification and assessment of potentially genotoxic impurities.
Each Cefadroxil-related product is rigorously characterized and delivered with a detailed Certificate of Analysis (COA) and comprehensive analytical data to ensure regulatory compliance. Upon request, we also offer EP/USP traceable standards. To maintain the highest quality standards, all materials are subject to periodic re-testing and continuous quality monitoring.
Cefadroxil
Cefadroxil Sulfoxide
Cefadroxil Monohydrate
Cefadroxil EP Impurity A
Cefadroxil EP Impurity A Hydrochloride
Cefadroxil EP Impurity A Sodium salt
Cefadroxil EP Impurity A Potassium salt
Cefadroxil EP Impurity A Sulfate salt
Cefadroxil EP Impurity B
Cefadroxil EP Impurity B Hydrochloride
Cefadroxil EP Impurity B Sodium salt
Cefadroxil EP Impurity C
Cefadroxil EP Impurity D
Cefadroxil EP Impurity E
Cefadroxil EP Impurity F
Cefadroxil EP Impurity G
Cefadroxil EP Impurity H
Cefadroxil Impurity 3
Cefadroxil USP Related Compound I
Cefadroxil S-sulfoxide (USP)
Cefadroxil Ethyl Homolog (USP)
N-Ethoxycarbonyl 7-ADCA
O-Ethoxycarbonyl Cefadroxil (USP)
Cefadroxil Dimer (USP)
O- Methoxycarbonyl Cefadroxil
N-Ethoxycarbonyl 7-ADCA (Na salt)
Cefadroxil Impurity 4
