NDFRT stands for the National Drug File - Reference Terminology, which is a comprehensive drug classification system used in healthcare and pharmacology. Developed by the United States Food and Drug Administration (FDA), NDFRT serves as a reference tool for organizing, categorizing, and standardizing drug-related information.
NDFRT is designed to provide a standardized framework for drug terminology, facilitating communication and interoperability between various healthcare systems, databases, and electronic health records. It includes a wide range of drug-related concepts, such as drug names, ingredient names, dosage forms, indications, contraindications, adverse effects, drug interactions, and therapeutic categories. The terminology is continually updated to reflect the latest information from FDA-approved drug labeling and other reliable sources.
This drug classification system enables healthcare professionals, researchers, and software developers to retrieve accurate and consistent drug information for a variety of purposes. It aids in drug safety monitoring, clinical decision support, drug utilization reviews, and drug data analysis. By using NDFRT, healthcare professionals can easily navigate and comprehend drug-related information, ensuring the safe and effective use of medications.
Overall, NDFRT provides a standardized and organized framework for drug information, improving the efficiency and accuracy of drug-related tasks in healthcare and facilitating better patient care.
