This brand name is authorized in Australia, Brazil, Israel, Turkey, United States
The drug NUVIGIL contains one active pharmaceutical ingredient (API):
1
Armodafinil
UNII V63XWA605I - ARMODAFINIL
|
Armodafinil is an indirect dopamine receptor agonist; both armodafinil and modafinil bind in vitro to the dopamine transporter and inhibit dopamine reuptake. Armodafinil (R-modafinil) has pharmacological properties similar to those of modafinil (a mixture of R- and S-modafinil), to the extent tested in animal and in vitro studies. |
Below package inserts are available for further reading:
Title | Information Source | Document Type | |
---|---|---|---|
NUVIGIL Tablet | FDA, National Drug Code (US) | MPI, US: SPL/PLR |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
N06BA13 | N Nervous system → N06 Psychoanaleptics → N06B Psychostimulants, agents used for ADHD and nootropics → N06BA Centrally acting sympathomimetics | |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: AU | Pharmaceutical Benefits Scheme | Identifier(s): 10912H, 10919Q, 10922W |
Country: BR | Câmara de Regulação do Mercado de Medicamentos | Identifier(s): 537521030009807, 537521030009907 |
Country: IL | מִשְׂרַד הַבְּרִיאוּת | Identifier(s): 7833, 7880 |
Country: TR | İlaç ve Tıbbi Cihaz Kurumu | Identifier(s): 8699638014026, 8699638014033, 8699638014132 |
Country: US | FDA, National Drug Code | Identifier(s): 63459-205, 63459-215, 63459-220, 63459-225 |
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