"49884-535-09" National Drug Code (NDC)

NDC Code	49884-535-09
Package Description	90 TABLET in 1 BOTTLE (49884-535-09)
Product NDC	49884-535
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Modafinil
Non-Proprietary Name	Modafinil
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120406
End Marketing Date	20200831
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA020717
Manufacturer	Par Pharmaceutical 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