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Azithromycin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Azithromycin 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 Azithromycin-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.
Azithromycin Dihydrate
Azithromycin EP Impurity A
Azithromycin EP Impurity B
Azithromycin EP Impurity C
Azithromycin EP Impurity D
Azithromycin EP Impurity E
Azithromycin EP Impurity F
Azithromycin EP Impurity G
Azithromycin EP Impurity H
Azithromycin EP Impurity I
Azithromycin EP Impurity J
Azithromycin EP Impurity K
Azithromycin EP Impurity L
Azithromycin EP Impurity M
Azithromycin EP Impurity N
Azithromycin EP Impurity O
Azithromycin Impurity P-Inhouse
Azithromycin Impurity Q
Azithromycin Impurity R
3-Hydroxy Azithromycinoic Acid Sodium Salt
Azaerythromycin A 11,12-hydrogen borate
3’-N-Demethyl-3’-N- (phenylsulfonyl) azithromycin
Azithromycin EP Impurity Q
Azithromycin Impurity 2
Azithromycin Impurity 3 Sodium Salt
Azithromycin Impurity 6
Azithromycin Impurity 7
Azithromycin Impurity Zy
N-Nitroso Azithromycin EP Impurity M
Azithromycin
