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  1. What are the four (4) key features of a drug's generic name? 1) Non-proprietary 2) Name given to drug before it becomes official 3) May be used in all countries by all manufacturers 4) No capitalization What are the two (2) key features of a drug's official name? 1) Name listed in "The United States Pharmacopeia National Formulary"

  2. A. This is the proprietary name of the drug given by the manufacturer that is trademarked. B. This is the common name by which most everyone refers to the drug. C. This is the name given to the drug based on the chemical structure. D. This is a non-proprietary name given by the United States Adopted Name Council.

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    What is a proprietary drug?

    What are some facts about the nomenclature of drugs prevailing in USA?

    Why is safety important in the naming of a proprietary drug?

    How is the chemical name of a drug decided?

  4. Feb 21, 2012 · After being approved by WHO, the drug is assigned an international nonproprietary name i. e. generic name. The USAN council adheres to a list of established guidelines in name selection. The most important criterion considered when issuing a generic name is the usefulness of that name to health care providers.

  5. Non-Proprietary Name: Semaglutide Drug Use Information Semaglutide is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes. Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems.

  6. Proprietary drug are chemicals used for medicinal purposes which are formulated or manufactured under a name protected from competition through trademark or patent. The invented drug is usually still considered proprietary even if the patent expired. When a patent expires, generic drugs may be developed and released legally.

  7. A proprietary name assigned to a drug by its manufacturer that is registered as part of the drug's identity. United States Pharmacopeia A compendium, recognized officially by the federal Food and Drug administration that contains descriptions, uses, strengths, and standards of purity for selected drugs and guidance for related standards of ...