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Celecoxib
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Celecoxib 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 Celecoxib-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.
Celecoxib
Celecoxib EP Impurity A
Celecoxib EP Impurity B
Celecoxib 2-Methyl Analog
Celecoxib Carboxylic Acid
Celecoxib Hydroxymethyl Analog
Celecoxib Hydrazine Impurity
Celecoxib Related Compound 1
Celecoxib Related Compound 3
Celecoxib Related Compound 4
Celecoxib Related Compound 7
Celecoxib Impurity 3
Celecoxib Impurity 4
Celecoxib Impurity 5
Celecoxib Impurity 6
Celecoxib Impurity 7
Celecoxib Impurity 8
Celecoxib Impurity 9
Celecoxib Impurity 10
Celecoxib Impurity 11
Celecoxib Impurity 12
Celecoxib Impurity 13
Celecoxib Impurity 14
Celecoxib Impurity 15
Celecoxib Impurity 16
Celecoxib Impurity 17
Celecoxib Impurity 18
Celecoxib Impurity 19
Celecoxib Impurity 20
Celecoxib Trifluro Impurity
Celecoxib Impurity 21
Celecoxib Impurity 22
Celecoxib Diketo schiff's base-II Impurity
Celecoxib Impurity 23
