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Roflumilast
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Roflumilast 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 Roflumilast-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.
Roflumilast
Roflumilast USP Related Compound B
Roflumilast Dihydroxy Impurity
Roflumilast N-Oxide
Roflumilast Dicyclopropylmethoxy Impurity
Roflumilast Carboxylic Acid Impurity
Roflumilast USP Related Compound A
5-Dechloro Roflumilast
Roflumilast Dimer
Roflumilast KSM-II Bromo Compound
Roflumilast KSM-I Acid compound
Roflumilast Impurity 1
Roflumilast USP Related Compound E
Roflumilast Impurity 3
Roflumilast Impurity 4
Roflumilast Impurity 5
Roflumilast Impurity 6
Roflumilast Impurity 7
Roflumilast Impurity 8
Roflumilast Impurity 9
Roflumilast Impurity 10
Roflumilast Impurity 11
Roflumilast Impurity 12
Roflumilast Impurity 13
Roflumilast Impurity 14
