Cytarabine EP Impurity H (HCl Salt), also known as Cyclocytidine hydrochloride ;Ancitabine hydrochloride ; 2,2′-O-Cyclocytidine hydrochloride is a highly characterized reference material. It fully complies with stringent regulatory standards, including those set by USP, EMA, JP, and BP. This product is essential for use in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial production of Cytarabine. Moreover, it comes with a detailed Structure Elucidation Report (SER), ensuring its accuracy and reliability for a wide range of analytical applications.“ Aceclofenac EP Impurity B (CAS No: 15307-78-5) or Aceclofenac Impurity B / Diclofenac Methyl Ester is a degradation product of Aceclofenac that reduces joint inflammation, pain intensity, and the duration of morning stiffness in rheumatoid arthritis patients.
References
Karbhari, PradnyaA, et al. “RP-LC Gradient Elution Method for Simultaneous Determination of Thiocolchicoside, Aceclofenac and Related Impurities in Tablet Formulation.” Journal of Pharmacy and Bioallied Sciences, vol. 6, no. 4, 2014, p. 246, https://doi.org/10.4103/0975-7406.142955. Dooley, Mukta, et al. “Aceclofenac.” Drugs, vol. 61, no. 9, 2001, pp. 1351–78, https://doi.org/10.2165/00003495-200161090-00012.
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