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.
(N,N-Didemethyl)-1-Hydroxy-Sibutramine
Benzyl Sibutramine
Chloro-Sibutramine HCl
Homo Sibutramine
N,N-Didesmethyl Sibutramine
N-Desmethyl Sibutramine
N-Formyl N,N-Didesmethyl Sibutramine
Sibutramine
Sibutramine Carbamic Acid Impurity 1
Sibutramine Hydrochloride Monohydrate
Sibutramine Hydrochloride Related Compound A
Sibutramine Hydrochloride Related Compound B
Sibutramine Hydrochloride Related Compound C
Sibutramine Hydrochloride Related Compound D
Sibutramine Impurity 1
Sibutramine Impurity 2
Sibutramine Impurity 3
Sibutramine Impurity E
Sibutramine Impurity F
Sibutramine Impurity H
Sibutramine Impurity I
Sibutramine Impurity J
Sibutramine Related Compound 1
Sibutramine N-Oxide
