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What is a non-proprietary name?
What is a non-proprietary name for a drug?
What is a proprietary name of a drug?
Can a drug have more than one non-proprietary name?
Mar 25, 2024 · 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 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 ...
Feb 21, 2023 · The USAN Council, the WHO’s International Nonproprietary Names (INN) expert group, and a medication’s manufacturer must agree on a generic name. The generic name selection process typically occurs in early phases of clinical trials. A generic name has a few defining elements, such as a common stem.
Jun 4, 2013 · The United States Adopted Names Council is responsible for selecting a United States Adopted Name (USAN) for drugs marketed in the U.S." Outside the U.S., the World Health Organization develops the International Nonproprietary Name (INN ), but through coordination with European and Japanese naming organizations as well as USAN, according to the ...
Generic (official) name . Brand (proprietary, trademark, or trade) name. The generic name is assigned, in the United States, by an official body—the United States Adopted Names (USAN) Council. The brand name is developed by the company requesting approval for the drug and identifies it as the exclusive property of that company.
Apr 10, 2020 · The International Nonproprietary Name (INN) is the official generic, non-proprietary name given to a pharmaceutical, such as paracetamol. In the US, there is also the USAN, an additional non-proprietary name selected by a council to ensure ‘safety, consistency and logic’.
Jan 18, 2017 · The Guidance applies to “originator product [s], related biological product [s] 1, and biosimilar product [s].”. Under the FDA’s current thinking, the naming convention would be both prospective and retrospective in effect, and would apply to both newly licensed and previously licensed products.
