Armodafinil: Difference between revisions
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Revision as of 19:22, 8 July 2014
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Clinical data | |
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Pregnancy category |
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Routes of administration | Oral |
ATC code | |
Legal status | |
Legal status |
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Pharmacokinetic data | |
Metabolism | Hepatic, including CYP3A4 and other pathways |
Elimination half-life | 12-15 hrs |
Excretion | Urine (as metabolites) |
Identifiers | |
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CAS Number | |
PubChem CID | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C15H15NO2S |
Molar mass | 273.351 |
Armodafinil (Nuvigil®) is an eugeroic drug produced by the pharmaceutical company Cephalon Inc., which was approved by the FDA on June 15, 2007.
Cephalon plans to conduct clinical trials evaluating the use of Nuvigil as a treatment for serious medical conditions such as bipolar depression, cognition associated with schizophrenia, and excessive sleepiness and fatigue in conditions such as Parkinson's disease and cancer.
Nuvigil is protected by a U.S. patent expiring in 2023 that claims the Form 1 polymorph of armodafinil.
Pill Images
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|Page Name=Armodafinil |Pill Name=Nuvigil_NDC_634590205.jpg |Drug Name=Nuvigil |Pill Ingred=armodafinil[armodafinil]|+sep=; |Pill Imprint=C;205 |Pill Dosage=50 mg |Pill Color=White|+sep=; |Pill Shape=Round |Pill Size (mm)=6 |Pill Scoring=1 |Pill Image= |Drug Author=Cephalon, Inc. |NDC=634590205
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{{#subobject:
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{{#subobject:
|Page Name=Armodafinil |Pill Name=Nuvigil_NDC_634590215.jpg |Drug Name=Nuvigil |Pill Ingred=armodafinil[armodafinil]|+sep=; |Pill Imprint=C;215 |Pill Dosage=150 mg |Pill Color=White|+sep=; |Pill Shape=Oval |Pill Size (mm)=13 |Pill Scoring=1 |Pill Image= |Drug Author=Cephalon, Inc. |NDC=634590215
}}
See also
External links
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