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  1. pharmacologymentor.com › drug-nomenclatureDrug Nomenclature: Drug Naming system | Pharmacology Mentor

    Mar 25, 2024 · Non-Proprietary Name. 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).

  2. en.wikipedia.org › wiki › InternationalInternational nonproprietary name - Wikipedia

    An international nonproprietary name ( INN) is an official generic and nonproprietary name given to a pharmaceutical drug or an active ingredient. [2] INNs are intended to make communication more precise by providing a unique standard name for each active ingredient, to avoid prescribing errors. [1] The INN system has been coordinated by the ...

    • paracetamol [11]
    • 对乙酰氨基酚 ( zh )
    • paracetamol [12]

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  4. en.wikipedia.org › wiki › Drug_nomenclatureDrug nomenclature - Wikipedia

    Drug nomenclature. 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 ...

    Stem
    Drug Class
    Example
    -vir
    Antiviral drug [2]
    aciclovir, oseltamivir
    -cillin
    Penicillin -derived antibiotics
    penicillin, carbenicillin, oxacillin [8]
    cef-
    Cephem -type antibiotics
    cefazolin
    -mab
    Monoclonal antibodies [2]
    trastuzumab, ipilimumab

    See full list on en.wikipedia.org

  5. www.fda.gov › media › 134015Drug Product Nomenclature - U.S. Food and Drug Administration

    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 ...

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  7. www.finnegan.com › en › insightsSummary of FDA Guidance on the Nonproprietary Naming of ...

    Jan 18, 2017 · On January 12, 2017, the U.S. Food and Drug Administration (“FDA”) released a final Guidance for Industry, Nonproprietary Naming of Biological Products, as part of the Agency’s ongoing efforts to implement the Biologics Price Competition and Innovation Act (BPCIA) of 2009.

  8. www.cnn.com › 2016/11/25 › healthThe art and science of naming prescription drugs | CNN

    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.

  9. www.pharmanaming.com › 06 › The-Drug-Naming-ProcessThe Drug Naming Process - pharma naming

    Jun 6, 2020 · Drugs often have several names. A marketed drug may have up to four different types of names: a chemical name, a company name, a generic name, and a brand name. Chemical name: When a drug is first discovered, it is given a chemical name. This describes the atomic or molecular structure of the drug. The chemical name is thus usually too complex ...

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