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Terazosin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Terazosin 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 Terazosin-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.
Terazosin HCl
Terazosin Hydrochloride Dihydrate
Terazosin EP Impurity A
Terazosin EP Impurity B
Terazosin EP Impurity C
Terazosin EP Impurity D
Terazosin EP Impurity E
Terazosin EP Impurity F
Terazosin EP Impurity G
Terazosin EP Impurity H
Terazosin EP Impurity I
Terazosin EP Impurity J
Terazosin EP Impurity K
Terazosin EP Impurity L
Terazosin EP Impurity M
Terazosin EP Impurity N
Terazosin EP Impurity O
Terazosin Impurity 1
Terazosin Impurity 2
Terazosin
