ARMODAFINIL

Product NDC
72189-261
11-digit product format
721890261
Labeler code
72189
Product ID
72189-261_2c28fdcb-8329-f51c-e063-6394a90a2fe2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ARMODAFINIL
Dosage form
TABLET
Route
ORAL
Labeler
direct rx
Application
NDA021875
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2021-09-13
Substance
ARMODAFINIL
Active strength
250 mg/1
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
ARMODAFINIL
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ARMODAFINIL250 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiV63XWA605I
Rxcui724861

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bf31ebd7-fd9d-472c-88e1-94944f023ec0Product name320190628

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72189-261-30ARMODAFINIL30 in 1 BOTTLETABLET304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72189-261ARMODAFINIL TABLET [DIRECT RX]4Current NDC, Legacy NDC, 1 package rows20250121_b1ba1cdd-cf57-7a8c-e053-2a95a90a2c19.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
724861armodafinil 250 MG Oral TabletPSNb1ba1cdd-cf57-7a8c-e053-2a95a90a2c194
724861armodafinil 250 MG Oral TabletSCDb1ba1cdd-cf57-7a8c-e053-2a95a90a2c194

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72189-261-307218902613030 TABLET in 1 BOTTLE (72189-261-30) 30 tablet2021-09-130000-00-00NoNoCurrent