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Almotriptan
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Almotriptan 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 Almotriptan-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.
Almotriptan
Almotriptan HCl
Almotriptan EP Impurity A
Almotriptan EP Impurity A (HCl)
Almotriptan EP Impurity B
Almotriptan EP Impurity C
Almotriptan EP Impurity D
Almotriptan EP Impurity E
Almotriptan EP Impurity E (HCl)
Almotriptan EP Impurity F
Almotriptan N-Dimer
Almotriptan N-Hydroxy Methyl Impurity
Almotriptan N-Isopropyl Impurity
Spiro Almotriptan
2-Hydroxyalmotriptan
Almotriptan Aniline Precursor
Almotriptan Hydrazine Precursor
Almotriptan Tetrahydro Indole Impurity
Almotriptan Methyl Tetrahydro Indole Impurity
Almotriptan Impurity 1
Almotriptan Nitroso Impurity 1
N-Nitroso Spiro Almotriptan
N-Nitroso Almotriptan EP Impurity A
