"0591-3500-01" National Drug Code (NDC)

NDC Code	0591-3500-01
Package Description	100 TABLET in 1 BOTTLE, PLASTIC (0591-3500-01)
Product NDC	0591-3500
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Modafinil
Non-Proprietary Name	Modafinil
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130403
End Marketing Date	20211130
Marketing Category Name	ANDA
Application Number	ANDA076715
Manufacturer	Actavis Pharma, Inc.
Substance Name	MODAFINIL
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Central Nervous System Stimulation [PE],Increased Sympathetic Activity [PE],Sympathomimetic-like Agent [EPC]
DEA Schedule	CIV