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Glimepiride
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Glimepiride 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 Glimepiride-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.
Glimepiride
Glimepiride EP Impurity A
Glimepiride EP Impurity B
Glimepiride EP Impurity C
Glimepiride EP Impurity D
Glimepiride EP Impurity E
Glimepiride EP Impurity F
Glimepiride EP Impurity G
Glimepiride EP Impurity H
Glimepiride EP Impurity I
Glimepiride EP Impurity J
Glimepiride meta-Ester Impurity
Glimepiride Phenylethyl Impurity
Glimepiride Sulfonamide ortho-Isomer
Glimepiride Ethyl Ester Impurity
trans-Hydroxy Glimepiride
trans-Carboxylic Acid Glimepiride
3-(Ethyl-d5)-1,5-dihydro-4-methyl-2H-pyrrol-2-one
Glimepiride System Suitability Mixture
Glimepiride Impurity 1
