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  1. Proprietary and non-proprietary name If a drug does not have a proprietary name, the established name of the drug should be included in the proprietary name field Dosage form and route of ...

  2. Brand Name (or proprietary drug name): C.01.001.(1) of the Food and Drug Regulations states that a "brand name" means, with reference to a drug, the name, whether or not including the name of any manufacturer, corporation, partnership or individual, in English or French, that is assigned to the drug by its manufacturer,

  3. 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.

  4. Feb 08, 2017 · C ialis, Eliquis, Jevtana, Xgeva. These drug names may sound silly, but the process of creating and testing them is anything but. With more than 30,000 proprietary drugs in the United States alone ...

  5. Jan 25, 2012 · The Generic Pharmaceutical Association requests that the U.S. Food and Drug Administration assign the same non-proprietary name to a biosimilar as the one held by its reference biologic. FDA has not articulated a policy for naming of biologics, biosimilars and interchangeable biosimilars, although they asked for input on the topic in the Public Meetings and Dockets surrounding the issuance of ...

  6. nonprescription drugs: drugs that can be obtained without a medical prescription; this is the Canadian term for what in the United States are called over the counter medications . There are three groups of nonprescription medications in Canada: (1) The first group includes proprietary medications that may be purchased in any retail outlet and ...

  7. Also known as the non-proprietary name Generic or generic name This is an artificial sweetener sometimes included in sugar-free syrups but should never be given to dogs

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