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.
5-Dechloro Roflumilast
Roflumilast Carboxylic Acid Impurity
Roflumilast Dicyclopropylmethoxy Impurity
Roflumilast Dihydroxy Impurity
Roflumilast Dimer
Roflumilast Impurity 1
Roflumilast Impurity 10
Roflumilast Impurity 11
Roflumilast Impurity 12
Roflumilast Impurity 13
Roflumilast Impurity 14
Roflumilast Impurity 3
Roflumilast Impurity 4
Roflumilast Impurity 5
Roflumilast Impurity 6
Roflumilast Impurity 7
Roflumilast Impurity 8
Roflumilast Impurity 9
Roflumilast KSM-I Acid compound
Roflumilast KSM-II Bromo Compound
Roflumilast N-Oxide
Roflumilast USP Related Compound A
Roflumilast USP Related Compound B
Roflumilast USP Related Compound E
Roflumilast
