"55253-802-90" National Drug Code (NDC)

NDC Code	55253-802-90
Package Description	90 TABLET in 1 BOTTLE (55253-802-90)
Product NDC	55253-802
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Modafinil
Non-Proprietary Name	Modafinil
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120329
End Marketing Date	20270228
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA020717
Manufacturer	CIMA LABS 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