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Naloxone
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Naloxone 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 Naloxone-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.
Naltrexone
Naltrexone Hydrochloride
Naltrexone EP Impurity A
Naltrexone EP Impurity B
Naltrexone EP Impurity C
Naltrexone EP Impurity D
Naltrexone EP Impurity E
Naltrexone EP Impurity F
Naloxone
Naloxone HCl
Naloxone EP Impurity A
Naloxone EP Impurity B
Naloxone EP Impurity C
Naloxone EP Impurity D
Naloxone EP Impurity E
Naloxone EP Impurity F
Naloxone EP Impurity G
Naloxone Impurity 1
O-Propyl Naloxone Enolether
N-Nitroso Naloxone EP Impurity A
Naloxone Impurity 3
Naloxone Impurity 4
Naloxone-D5
Naloxone N-Oxide
Naloxone Hydroxylamine
Naloxone Amide
10-Oxo Naloxone
Carbamat Noroxymorphone
