Eltrombopag Amino Impurity

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Eltrombopag amino impurities are monitored in pharmaceutical formulations to ensure drug safety and efficacy, as they can arise during synthesis or storage. Their detection and control are critical for regulatory compliance and maintaining the quality of eltrombopag-containing medications.