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      • The non-proprietary name of a drug is the name accepted by a competent scientific body or authority, such as the USAN or BAN. The non-proprietary names of newer drugs are kept uniform by an agreement to use the Recommended International Nonproprietary Name (rINN) in all member countries of the World Health Organization (WHO).
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  2. Mar 25, 2024 · The non-proprietary name of a drug is the name accepted by a competent scientific body or authority, such as the USAN or BAN. The non-proprietary names of newer drugs are kept uniform by an agreement to use the Recommended International Nonproprietary Name (rINN) in all member countries of the World Health Organization (WHO).

    • Overview of Generic Naming
    • Usan Program History
    • What Usan Names
    • What Names Mean
    • Balancing The Needs of Firms and Patients
    • Conclusions

    The assignment of generic names to pharmaceuticals in development is an important prerequisite to marketing a drug. The United States Adopted Names (USAN) Program, which assigns generic (nonproprietary) names to all active drug ingredients in the United States, is the result of a long-time partnership between the American Medical Association (AMA),...

    The USAN Program originated with the AMA’s Council on Pharmacy and Chemistry, which was created in 1905 to evaluate drugs and to try to eliminate quackery in medications.3 In 1938, the Food, Drug, and Cosmetic Act established federal regulatory authority over drugs, including requiring proof of safety,4 but the AMA’s Council on Pharmacy and Chemist...

    Over 10 000 drugs have received nonproprietary names since the WHO, AMA, USP, and APhA began assigning names to drugs,11 and they are listed in online databases such as the USP Dictionary of USAN and International Drug Names.1In 2018, the USAN program named 198 substances. The number of USAN adoptions fluctuates from year to year but has grown stea...

    In naming drugs, the most important considerations are avoiding drug names that are too similar to existing names—and therefore might compromise patient safety—and making sure the drug name communicates accurate information about the action or use of the substance. Over time, the USAN and INN nomenclature scheme has developed into a system for clas...

    As with any complex multiparty negotiation, there can be disagreements. The USAN Council’s focus on patient safety, access to new drugs, and communicating necessary information about drugs through the generic name is sometimes in conflict with the desires of pharmaceutical companies to create either a certain message about their drugs through the g...

    For decades, assignment of a USAN has been a key step in the development and marketing of a new active pharmaceutical ingredient, because a substance cannot be marketed in the United States without a name. The primary goals of the USAN Council are to facilitate the safe use of medications by assigning names that are unlikely to result in medical er...

    • Gail B Karet
    • 2019
  3. Drug nomenclature is the systematic naming of drugs, especially pharmaceutical drugs. In the majority of circumstances, drugs have 3 types of names: chemical names, the most important of which is the IUPAC name; generic or nonproprietary names, the most important of which are international nonproprietary names (INNs); and trade names, which are ...

    Stem
    Drug Class
    Example
    aciclovir, oseltamivir
    Penicillin-derived antibiotics
    penicillin, carbenicillin, oxacillin
    Cephem-type antibiotics
    trastuzumab, ipilimumab
  4. Feb 21, 2023 · The USAN Council, the WHO’s International Nonproprietary Names (INN) expert group, and a medication’s manufacturer must agree on a generic name. The generic name selection process typically occurs in early phases of clinical trials. A generic name has a few defining elements, such as a common stem.

  5. Nov 25, 2016 · “This step assures that there is one non-proprietary (generic) name throughout the world for the drug,” explained Stephanie C. Shubat, director of the Adopted Name Council.

  6. 18 [Drug] If the Active Ingredient is a: •“Non-salt” (e.g. ester, chelate, complex) –use the entire drug substance name •Salt –generally, use the name of active moiety –sometimes ...

  7. Apr 10, 2020 · The American Medical Association (AMA) has issued guidelines on naming using United States Adopted Names (USAN), which are unique non-proprietary names assigned to pharmaceuticals sold in the US. Non-proprietary names are names for products that are not subject to trademark rights.