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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).
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 ...
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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.
Apr 13, 2021 · The World Health Organization assigns international nonproprietary names (INN), also known as common names, to compounds upon request from drug developers. Structures of INNs are publicly available and represent a source, albeit underused, to understand trends in drug research and development. Here, we explain how a common drug name is composed and analyze chemical entities from 2000 to 2021 ...
- Marta Serafini, Sarah Cargnin, Alberto Massarotti, Gian Cesare Tron, Tracey Pirali, Armando A Genazz...
- 2021
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 ...
Jun 6, 2020 · A company that is developing a new drug will use a company code to identify it within the company. The company code name for a drug is used prior to designation of a generic name. Generic & Brand names: When a drug is approved by the FDA, it is given a Generic (official) name and a Brand (proprietary or trademark or trade) name.
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.
