Diclofenac EP Impurity D also known as , Diclofenac Related Compound D in various pharmacopoeias, is a highly characterized standard. It meets strict regulatory requirements set by USP, EMA, JP, and BP, making it a crucial component in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial production of Diclofenac . To ensure precision and reliability in analytical applications, this impurity standard is supplied with a detailed Structure Elucidation Report (SER), offering valuable insights for method development and quality control. Diclofenac EP Impurity D is a bromide impurity of Diclofenac. Diclofenac is a synthetic nonsteroidal anti-inflammatory drug. This drug is well-known and commercially available on the market in various pharmaceutical forms.
References
Galmier, Marie-Josèphe, et al. “Identification of Degradation Products of Diclofenac by Electrospray Ion Trap Mass Spectrometry.â€Â Journal of Pharmaceutical and Biomedical Analysis, vol. 38, no. 4, July 2005, pp. 790–96, https://doi.org/10.1016/j.jpba.2005.02.016.
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