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Chemistry

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Also known as: 112111-43-0, Nuvigil, (r)-modafinil, (-)-modafinil, (r)-(-)-modafinil, Cep-10953
Molecular Formula
C15H15NO2S
Molecular Weight
273.4  g/mol
InChI Key
YFGHCGITMMYXAQ-LJQANCHMSA-N
FDA UNII
V63XWA605I

Armodafinil
A benzhydryl acetamide compound, central nervous system stimulant, and CYP3A4 inducing agent that is used in the treatment of NARCOLEPSY and SLEEP WAKE DISORDERS.
1 2D Structure

Armodafinil

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
2-[(R)-benzhydrylsulfinyl]acetamide
2.1.2 InChI
InChI=1S/C15H15NO2S/c16-14(17)11-19(18)15(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,15H,11H2,(H2,16,17)/t19-/m1/s1
2.1.3 InChI Key
YFGHCGITMMYXAQ-LJQANCHMSA-N
2.1.4 Canonical SMILES
C1=CC=C(C=C1)C(C2=CC=CC=C2)S(=O)CC(=O)N
2.1.5 Isomeric SMILES
C1=CC=C(C=C1)C(C2=CC=CC=C2)[S@](=O)CC(=O)N
2.2 Other Identifiers
2.2.1 UNII
V63XWA605I
2.3 Synonyms
2.3.1 MeSH Synonyms

1. 2 Benzhydrylsulfinylacetamide

2. 2-((diphenylmethyl)sulfinyl)acetamide

3. 2-((r)-(diphenylmethyl)sulfinyl)acetamide

4. 2-(benzhydrylsulfinyl)acetamide

5. 2-benzhydrylsulfinylacetamide

6. Alertec

7. Benzhydrylsulfinylacetamide

8. Crl 40476

9. Crl-40476

10. Modafinil

11. Modiodal

12. Nuvigil

13. Provigil

14. R Modafinil

15. R-modafinil

16. Sparlon

2.3.2 Depositor-Supplied Synonyms

1. 112111-43-0

2. Nuvigil

3. (r)-modafinil

4. (-)-modafinil

5. (r)-(-)-modafinil

6. Cep-10953

7. Crl 40982

8. Modafinil, (r)-

9. R-(-)-modafinil

10. 2-[(r)-(diphenylmethyl)sulfinyl]acetamide

11. (-)-(r)-modafinil

12. Cep 10953

13. Cep-10952

14. Crl-40982

15. V63xwa605i

16. Chembl1201192

17. Chebi:77590

18. Nsc-751850

19. Nsc-758711

20. (-)-2-((r)-(diphenylmethyl)sulfinyl)acetamide

21. Acetamide, 2-((diphenylmethyl)sulfinyl)-, (-)-

22. Armodafinil [inn]

23. (-)-2-[(r)-(diphenylmethyl)sulfinyl]acetamide

24. Armodafinil [usan:inn]

25. Armodafinilo

26. Armodafinilum

27. Unii-v63xwa605i

28. L-modafinil

29. (-) Modafinil

30. Nuvigil (tn)

31. Armodafinil (usan/inn)

32. Armodafinil [usan]

33. Armodafinil [vandf]

34. Armodafinil [mart.]

35. Schembl34489

36. Armodafinil [usp-rs]

37. Armodafinil [who-dd]

38. Zinc6156

39. Armodafinil, >=98% (hplc)

40. Armodafinil [orange Book]

41. Dtxsid90920667

42. 2-[(r)-benzhydrylsulfinyl]acetamide

43. Bdbm50336892

44. Akos030211019

45. At22562

46. Ccg-230228

47. Cs-0665

48. Db06413

49. Nsc 751850

50. Nsc 758711

51. 2-[(r)-diphenylmethanesulfinyl]acetamide

52. Hy-15201

53. (-)-2r-[(diphenylmethyl)sulfinyl]acetamide

54. S4645

55. D03215

56. Q418913

57. Acetamide, 2-((r)-(diphenylmethyl)sulfinyl)-

2.4 Create Date
2006-10-24
3 Chemical and Physical Properties
Molecular Weight 273.4 g/mol
Molecular Formula C15H15NO2S
XLogP31.7
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Exact Mass273.08234989 g/mol
Monoisotopic Mass273.08234989 g/mol
Topological Polar Surface Area79.4 Ų
Heavy Atom Count19
Formal Charge0
Complexity302
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Drug and Medication Information
4.1 Drug Information
1 of 4  
Drug NameArmodafinil
PubMed HealthArmodafinil (By mouth)
Drug ClassesCNS Stimulant
Drug LabelNUVIGIL (armodafinil) is a wakefulness-promoting agent for oral administration. Armodafinil is the R-enantiomer of modafinil which is a mixture of the R- and S-enantiomers. The chemical name for armodafinil is 2-[(R)-(diphenylmethyl)sulfinyl]acetam...
Active IngredientArmodafinil
Dosage FormTablet
Routeoral; Oral
Strength2500mg; 200mg; 250mg; 100mg; 50mg; 150mg
Market StatusTentative Approval; Prescription
CompanyWatson Labs; Mylan Pharms; Teva Pharms Usa; Lupin

2 of 4  
Drug NameNuvigil
PubMed HealthArmodafinil (By mouth)
Drug ClassesCNS Stimulant
Drug LabelNUVIGIL (armodafinil) is a wakefulness-promoting agent for oral administration. Armodafinil is the R-enantiomer of modafinil which is a mixture of the R- and S-enantiomers. The chemical name for armodafinil is 2-[(R)-(diphenylmethyl)sulfinyl]acetam...
Active IngredientArmodafinil
Dosage FormTablet
RouteOral
Strength200mg; 250mg; 150mg; 50mg
Market StatusPrescription
CompanyCephalon

3 of 4  
Drug NameArmodafinil
PubMed HealthArmodafinil (By mouth)
Drug ClassesCNS Stimulant
Drug LabelNUVIGIL (armodafinil) is a wakefulness-promoting agent for oral administration. Armodafinil is the R-enantiomer of modafinil which is a mixture of the R- and S-enantiomers. The chemical name for armodafinil is 2-[(R)-(diphenylmethyl)sulfinyl]acetam...
Active IngredientArmodafinil
Dosage FormTablet
Routeoral; Oral
Strength2500mg; 200mg; 250mg; 100mg; 50mg; 150mg
Market StatusTentative Approval; Prescription
CompanyWatson Labs; Mylan Pharms; Teva Pharms Usa; Lupin

4 of 4  
Drug NameNuvigil
PubMed HealthArmodafinil (By mouth)
Drug ClassesCNS Stimulant
Drug LabelNUVIGIL (armodafinil) is a wakefulness-promoting agent for oral administration. Armodafinil is the R-enantiomer of modafinil which is a mixture of the R- and S-enantiomers. The chemical name for armodafinil is 2-[(R)-(diphenylmethyl)sulfinyl]acetam...
Active IngredientArmodafinil
Dosage FormTablet
RouteOral
Strength200mg; 250mg; 150mg; 50mg
Market StatusPrescription
CompanyCephalon

4.2 Drug Indication

Investigated for use/treatment in sleep disorders, obstructive sleep apnea, schizophrenia and schizoaffective disorders, depression, and bipolar disorders.


FDA Label


5 Pharmacology and Biochemistry
5.1 MeSH Pharmacological Classification

Central Nervous System Stimulants

A loosely defined group of drugs that tend to increase behavioral alertness, agitation, or excitation. They work by a variety of mechanisms, but usually not by direct excitation of neurons. The many drugs that have such actions as side effects to their main therapeutic use are not included here. (See all compounds classified as Central Nervous System Stimulants.)


Cytochrome P-450 CYP3A Inducers

Drugs and compounds that induce the synthesis of CYTOCHROME P-450 CYP3A. (See all compounds classified as Cytochrome P-450 CYP3A Inducers.)


Wakefulness-Promoting Agents

A specific category of drugs that prevent sleepiness by specifically targeting sleep-mechanisms in the brain. They are used to treat DISORDERS OF EXCESSIVE SOMNOLENCE such as NARCOLEPSY. Note that this drug category does not include broadly-acting central nervous system stimulants such as AMPHETAMINES. (See all compounds classified as Wakefulness-Promoting Agents.)


5.2 ATC Code

N - Nervous system

N06 - Psychoanaleptics

N06B - Psychostimulants, agents used for adhd and nootropics

N06BA - Centrally acting sympathomimetics

N06BA13 - Armodafinil


5.3 Absorption, Distribution and Excretion

Absorption

Tmax is 2 hours when fasted and can be delayed approximately 2-4 hours by food, potentially affecting the onset of action.


Volume of Distribution

Apparent volume of distribution: 42L.


Clearance

The oral clearance of armodafinil is approximately 33 mL/min.


5.4 Metabolism/Metabolites

In vitro and in vivo data show that armodafinil undergoes hydrolytic deamidation, S-oxidation, and aromatic ring hydroxylation, with subsequent glucuronide conjugation of the hydroxylated products. Amide hydrolysis is the single most prominent metabolic pathway, with sulfone formation by cytochrome P450 (CYP) 3A4/5 being next in importance. The other oxidative products are formed too slowly in vitro to enable identification of the enzyme(s) responsible. Only two metabolites reach appreciable concentrations in plasma (i.e., R-modafinil acid and modafinil sulfone). Data specific to armodafinil disposition are not available.


5.5 Biological Half-Life

Terminal half-life is approximately 15 hours.


5.6 Mechanism of Action

Nuvigil (armodafinil) is a single-isomer of modafini. The exact mechanism of action is unknown. Armodafinil belongs to a class of drugs known as eugeroics, which are stimulants that provide long-lasting mental arousal. Pharmacologically, armodafinil does not bind to or inhibit several receptors and enzymes potentially relevant for sleep/wake regulation. Armodafinil is not a direct- or indirect-acting dopamine receptor agonist. However, in vitro, both armodafinil and modafinil bind to the dopamine transporter and inhibit dopamine reuptake. [Medilexicon]


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05-Jan-2021
15-Oct-2024
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DOSAGE - TABLET;ORAL - 100MG **Federal Regist...DOSAGE - TABLET;ORAL - 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 21875

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DOSAGE - TABLET;ORAL - 150MG

USFDA APPLICATION NUMBER - 21875

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DOSAGE - TABLET;ORAL - 200MG

USFDA APPLICATION NUMBER - 21875

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DOSAGE - TABLET;ORAL - 250MG

USFDA APPLICATION NUMBER - 21875

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DOSAGE - TABLET;ORAL - 50MG

USFDA APPLICATION NUMBER - 21875

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ABOUT THIS PAGE

Nuvigil Manufacturers

A Nuvigil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nuvigil, including repackagers and relabelers. The FDA regulates Nuvigil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nuvigil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

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Nuvigil Suppliers

A Nuvigil supplier is an individual or a company that provides Nuvigil active pharmaceutical ingredient (API) or Nuvigil finished formulations upon request. The Nuvigil suppliers may include Nuvigil API manufacturers, exporters, distributors and traders.

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Nuvigil USDMF

A Nuvigil DMF (Drug Master File) is a document detailing the whole manufacturing process of Nuvigil active pharmaceutical ingredient (API) in detail. Different forms of Nuvigil DMFs exist exist since differing nations have different regulations, such as Nuvigil USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Nuvigil DMF submitted to regulatory agencies in the US is known as a USDMF. Nuvigil USDMF includes data on Nuvigil's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nuvigil USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Nuvigil suppliers with USDMF on PharmaCompass.

Nuvigil KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Nuvigil Drug Master File in Korea (Nuvigil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nuvigil. The MFDS reviews the Nuvigil KDMF as part of the drug registration process and uses the information provided in the Nuvigil KDMF to evaluate the safety and efficacy of the drug.

After submitting a Nuvigil KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Nuvigil API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Nuvigil suppliers with KDMF on PharmaCompass.

Nuvigil WC

A Nuvigil written confirmation (Nuvigil WC) is an official document issued by a regulatory agency to a Nuvigil manufacturer, verifying that the manufacturing facility of a Nuvigil active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Nuvigil APIs or Nuvigil finished pharmaceutical products to another nation, regulatory agencies frequently require a Nuvigil WC (written confirmation) as part of the regulatory process.

click here to find a list of Nuvigil suppliers with Written Confirmation (WC) on PharmaCompass.

Nuvigil NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Nuvigil as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Nuvigil API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Nuvigil as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Nuvigil and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nuvigil NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Nuvigil suppliers with NDC on PharmaCompass.

Nuvigil GMP

Nuvigil Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Nuvigil GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Nuvigil GMP manufacturer or Nuvigil GMP API supplier for your needs.

Nuvigil CoA

A Nuvigil CoA (Certificate of Analysis) is a formal document that attests to Nuvigil's compliance with Nuvigil specifications and serves as a tool for batch-level quality control.

Nuvigil CoA mostly includes findings from lab analyses of a specific batch. For each Nuvigil CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Nuvigil may be tested according to a variety of international standards, such as European Pharmacopoeia (Nuvigil EP), Nuvigil JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Nuvigil USP).

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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