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01 4AUROBINDO PHARMA LTD
02 3COREPHARMA
03 5LUPIN LTD
04 5MYLAN PHARMS INC
05 5NATCO PHARMA LTD
06 5NUVO PHARMS
07 5TEVA PHARMS USA INC
08 5WATSON LABS INC
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01 4TABLET; ORAL
02 33TABLET;ORAL
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01 6DISCN
02 22RX
03 9Blank
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01 32ARMODAFINIL
02 5NUVIGIL
01 23No
02 5Yes
03 9Blank
RLD : No
TE Code : AB
Brand Name : ARMODAFINIL
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Approval Date : 2012-06-01
Application Number : 200043
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ARMODAFINIL
Dosage Form : TABLET;ORAL
Dosage Strength : 150MG
Approval Date : 2012-06-01
Application Number : 200043
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ARMODAFINIL
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Approval Date : 2012-06-01
Application Number : 200043
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ARMODAFINIL
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG
Approval Date : 2019-05-09
Application Number : 200043
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ARMODAFINIL
Dosage Form : TABLET;ORAL
Dosage Strength : 200MG
Approval Date : 2019-05-09
Application Number : 200043
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Brand Name : NUVIGIL
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Approval Date : 2007-06-15
Application Number : 21875
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Brand Name : NUVIGIL
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 2009-03-26
Application Number : 21875
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Brand Name : NUVIGIL
Dosage Form : TABLET;ORAL
Dosage Strength : 150MG
Approval Date : 2007-06-15
Application Number : 21875
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Brand Name : NUVIGIL
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Approval Date : 2007-06-15
Application Number : 21875
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Brand Name : NUVIGIL
Dosage Form : TABLET;ORAL
Dosage Strength : 200MG
Approval Date : 2009-03-26
Application Number : 21875
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF