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Naltrexone
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Naltrexone 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 Naltrexone-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
Naltrexone EP Impurity G
Naltrexone EP Impurity H
Naltrexone EP Impurity I
Naltrexone EP Impurity J
3-(O)-Acetyl Naltrexone Methobromide
3-O-Acetyl Naltrexone
3-(O)-Methylnaltrexone Methobromide
Methylnaltrexone Bromide
6β-Naltrexol
17S-Naltrexone Methobromide
Oxymorphone butenylbromide
10-Hydroxy Naltrexone
Naltrexone Aldol Dimer
Naltrexone D4
Δ7-Naltrexone
6β-Naltrexol D4
Naltrexone D3
6β-Naltrexol D3
2-Hydroxy-3-Methoxynaltrexone
2-Hydroxy-3-Methoxy-6Beta-Naltrexol
3-(O)-Acetyl Naltrexone
