Armodafinil

Product NDC
71335-0710
11-digit product format
713350710
Labeler code
71335
Product ID
71335-0710_d8558bc2-6354-454a-81e9-3fad93f276f5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Armodafinil
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA200751
Marketing category
ANDA
Marketing start
2016-11-28
Marketing end
0000-00-00
Substance
ARMODAFINIL
Active strength
250 mg/1
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71335-0710DDiscontinued by firm2026-07-31
excluded packagepackage71335-071071335-0710-1DDiscontinued by firm2026-07-31
excluded packagepackage71335-071071335-0710-2DDiscontinued by firm2026-07-31
excluded packagepackage71335-071071335-0710-3DDiscontinued by firm2026-07-31

Orange Book products#

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A200751-001ARMODAFINILARMODAFINIL50MGTABLET / ORAL2016-11-28
A200751-003ARMODAFINILARMODAFINIL150MGTABLET / ORAL2016-11-28
A200751-004ARMODAFINILARMODAFINIL200MGTABLET / ORAL2016-11-28
A200751-005ARMODAFINILARMODAFINIL250MGTABLET / ORAL2016-11-28

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0710-17133507100130 TABLET in 1 BOTTLE (71335-0710-1) 30 tablet2018-03-020000-00-00NoNoCurrent
71335-0710-27133507100228 TABLET in 1 BOTTLE (71335-0710-2) 28 tablet2018-03-020000-00-00NoNoCurrent
71335-0710-37133507100390 TABLET in 1 BOTTLE (71335-0710-3) 90 tablet2018-03-020000-00-00NoNoCurrent