Venkatasai is a leading innovator in the field of pharmaceutical reference standards, offering high-quality Reference Standards of Abacavir, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamines (N-NO products). Our Abacavir impurity reference standards play a vital role in pharmaceutical research, supporting product development, ANDA and DMF filings, quality control (QC), method validation, and stability studies. They are also instrumental in identifying unknown impurities and evaluating genotoxic potential. All Abacavir-related products are thoroughly characterized and supplied with comprehensive Certificates of Analysis (COA) and analytical data that comply with regulatory standards. EP/USP traceable standards can also be provided upon request. Furthermore, all supplied products undergo periodic re-testing to ensure continued quality and reliability.
10-Hydroxy Naltrexone
17S-Naltrexone Methobromide
2-Hydroxy-3-Methoxy-6Beta-Naltrexol
2-Hydroxy-3-Methoxynaltrexone
3-(O)-Acetyl Naltrexone
3-(O)-Acetyl Naltrexone Methobromide
3-(O)-Methylnaltrexone Methobromide
3-O-Acetyl Naltrexone
6β-Naltrexol D3
6β-Naltrexol D4
Methylnaltrexone Bromide
Naltrexone
Naltrexone Aldol Dimer
Naltrexone D3
Naltrexone D4
Naltrexone EP Impurity A
Naltrexone EP Impurity B
Naltrexone EP Impurity C
Naltrexone EP Impurity C (HCl salt)
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
Naltrexone Hydrochloride
Oxymorphone butenylbromide
Δ7-Naltrexone
