ARMODAFINIL

Product NDC: 59651-047
11-digit product format: 596510047
Labeler code: 59651
Product ID: 59651-047_a75b2046-1bc3-4ada-a593-7300665acdd6
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: ARMODAFINIL
Dosage form: TABLET
Route: ORAL
Labeler: AUROBINDO PHARMA LIMITED
Application: NDA021875
Marketing category: NDA
Marketing start: 2016-08-03
Marketing end: 2023-05-31
Substance: ARMODAFINIL
Active strength: 200 mg/1
DEA schedule: CIV
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59651-047-30	EA - Each	59651-047	c81519db-9fb0-4003-b901-afd4f8a6ca2d	1	2016-09-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59651-047-30	59651004730	30 TABLET in 1 BOTTLE (59651-047-30)	30 tablet	2016-08-03	2023-05-31	No	No	Current