Pronunciation: [ˌɛndˌiːsˈiː] (IPA) 
The abbreviation "NDC" can be spelled out using the International Phonetic Alphabet (IPA) as /ɛn di si/. This spelling represents the individual sounds of the three letters: "en" for the /ɛn/ sound, "di" for the /di/ sound, and "si" for the /si/ sound. Additionally, the IPA provides a consistent and precise way to describe the pronunciation of words, which can be particularly helpful for those learning English as a second language.
NDC, short for National Drug Code, is a unique numerical identifier used in the United States healthcare industry to identify and track drugs. It is a product identifier code, assigned by the Food and Drug Administration (FDA), which facilitates the identification and tracking of specific drugs.
The NDC code consists of a three-segment, 10-digit number. The first segment represents the manufacturer or distributor of the drug, whereas the second segment denotes the specific drug product itself. The third segment denotes the package size or type of the drug. This unique identification system enables pharmacies, hospitals, and healthcare providers to accurately differentiate between different drugs and to ensure patient safety by avoiding medication errors or confusion.
The NDC code is widely used and recognized within the healthcare industry, serving various important purposes. It enables accurate identification of drugs during prescribing, dispensing, and administering processes. It assists in drug inventory management, tracking, and billing procedures. Additionally, it facilitates drug safety research, post-marketing surveillance, and regulatory compliance. The code also aids in ensuring accurate and efficient reimbursement processes within the healthcare system.
Overall, the National Drug Code (NDC) is an essential component of the healthcare industry in the United States, providing a standardized and universal identification system for drugs that improves patient safety, assists in inventory management, facilitates billing processes, and supports regulatory compliance and research efforts.
