Armodafinil

Product NDC: 68180-571
11-digit product format: 681800571
Labeler code: 68180
Product ID: 68180-571_b4c0895d-90c6-4624-98fb-978e2c2893e3
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Armodafinil
Dosage form: TABLET
Route: ORAL
Labeler: Lupin Pharmaceuticals, Inc.
Application: ANDA200751
Marketing category: ANDA
Marketing start: 2016-11-28
Marketing end: 0000-00-00
Substance: ARMODAFINIL
Active strength: 150 mg/1
DEA schedule: CIV
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
bf31ebd7-fd9d-472c-88e1-94944f023ec0	Product name	3	20190628

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
68180-571-02	EA - Each	68180-571	183020eb-bd0e-43a4-857c-379ad41a7438	1	2016-12-07
68180-571-07	EA - Each	68180-571	df226364-23fc-4bb3-a8f2-2668f3ed05b8	1	2016-12-07

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
724859	armodafinil 150 MG Oral Tablet	PSN	7ea5430a-df28-e521-e053-2a91aa0a8f22	2
724859	armodafinil 150 MG Oral Tablet	SCD	7ea5430a-df28-e521-e053-2a91aa0a8f22	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
68180-571-02	68180057102	500 TABLET in 1 BOTTLE (68180-571-02)	500 tablet	2016-11-28	0000-00-00	No	No	Current
68180-571-07	68180057107	60 TABLET in 1 BOTTLE (68180-571-07)	60 tablet	2016-11-28	0000-00-00	No	No	Current