1500 ng/day is the U.S. FDA’s current Acceptable Intake (AI) limit for N-nitroso-bupropion (NDSRI). Refer to the FDA nitrosamine page for the latest guidance.
Bupropion Nitroso Impurity is an N-nitroso derivative of the secondary amine present in Bupropion | which is a highly characterized reference material that meets stringent regulatory standards set for nitrosamine compounds | including those set by USP | EMA | JP | and BP. This nitroso standard is essential for a variety of applications | such as analytical method development | method validation (AMV) | and Quality Control (QC) | particularly in the context of Bupropion production. It is suitable for use in both Abbreviated New Drug Applications (ANDA) and New Drug Applications (NDA). This nitrosamine standard helps establish detection limits | quantify impurity levels | and ensure trace nitroso impurities in pharmaceutical products remain within FDA and EMA safety limits.
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