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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 › Drug_nomenclatureDrug nomenclature - Wikipedia

    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 brand names.

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  4. journalofethics.ama-assn.org › article › how-doHow Do Drugs Get Named? | Journal of Ethics | American ...

    Of all the drugs named in 2018, 112 (57%) were chemical substances (organic molecules) or their salts or esters intended as drugs for human use. The USAN Program named 76 substances (38%) that were biological in nature, including gene therapies, cell therapies, oligonucleotides, monoclonal antibodies and antibody drug conjugates, and other ...

    • Gail B Karet
    • 2019

  5. www.goodrx.com › drugs › medication-basicsHow Do Drugs Get Named? - GoodRx

    Feb 21, 2023 · Key takeaways: Every medication has at least three names: a chemical name, a generic name, and a brand name. Several organizations are involved in naming medications. Pharmaceutical companies, the FDA, and the U.S. Adopted Names Council are three key examples. Medication names have to follow many rules, and this can make them sound complex.

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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.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 ...

  9. www.pharmapproach.com › drug-nomenclature-how-doesDrug Nomenclature: How Does A Drug Get Its Name?

    Oct 11, 2023 · Generic name. Drugs are also known by generic, non- proprietary or official names. This is the name given to a drug after it might have been found to be of therapeutic use. It is the name with which the drug is described in official books of reference like pharmacopoeias. It is also the name that is authoritatively accepted by a scientific body.