"57237-155-01" National Drug Code (NDC)

NDC Code	57237-155-01
Package Description	100 TABLET in 1 BOTTLE (57237-155-01)
Product NDC	57237-155
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Modafinil
Non-Proprietary Name	Modafinil
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120927
Marketing Category Name	ANDA
Application Number	ANDA202566
Manufacturer	Rising Pharma Holdings, 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