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Cefdinir
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Cefdinir 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 Cefdinir-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.
Cefdinir
Cefdinir (E)-Isomer (USP)
Cefdinir 3-Methyl Impurity (USP)
Cefdinir Isoxazole Analog (USP)
Cefdinir Lactone (USP)
Cefdinir Thiazolylacetyl Glycine Oxime Acetal Impurity (USP)
Cefdinir Thiazolylacetyl Glycine Oxime Impurity (USP)
Cefdinir USP Related Compound A (Na)
Cefdinir USP Related Compound B
Cefdinir Decarboxy Open Ring Lactone Impurity
Cefdinir Isoxazole Analog
Cefdinir 7-Epimer
Cefdinir Sulfoxide
Cefdinir glyoxalic analog
Cefdinir thiazine analog
O-Acetyl Cefdinir
N-Acetyl Cefdinir
7S Cefdinir Impurity
Trytil Cefdinir CFD-I IS
Cefdinir Impurity 1
Cefdinir Impurity 2
Cefdinir Impurity A
Cefdinir USP Related Compound A
Cefdinir Impurity 3
