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Determination of a Genotoxic NDMA Impurity Using the High-Resolution Agilent 6546 LC/Q-TOF in Ranitidine Drug Substance and Drug Products

 

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Application Note Pharma & Biopharma Determination of NDMA Impurity in Ranitidine Using the Agilent 6470 Triple Quadrupole LC/MS Detection of regulated genotoxic impurity from the drug manufacturing process Authors Chander Mani and Saikat Banerjee Agilent Technologies, Inc. Abstract Impurities in…
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Nitrosamine Impurities Application Guide Confidently Detect and Quantify Mutagenic Impurities in APIs and Drug Products Sartan-Based Losartan Valsartan Candesartan Telmisartan Metformin Ranitidine Nitrosamines are formed by chemical reactions that occur during API manufacturing whether from starting materials, intermediates, reactants, reuse…
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APPLICATION NOTE 73814 HRAM LC-MS method for the determination of nitrosamine impurities in drugs Authors: Hao Yang, Thermo Fisher Scientific, San Jose, CA, US Jon Bardsley, Thermo Fisher Scientific, Hemel Hempstead, UK Min Du, Thermo Fisher Scientific, Boston, MA, US…
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NDMA impurity in Ranitidine / LCMSTM-9030 Application News Detection and Quantitation of NDMA Impurity in Ranitidine Drug Substances and Products by LC-HRMS on LCMS-9030 Zhe Sun and Zhaoqi Zhan User Benefits  Determination of NDMA in ranitidine API and drug…
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