"57237-240-01" National Drug Code (NDC)

NDC Code	57237-240-01
Package Description	100 CAPSULE in 1 BOTTLE (57237-240-01)
Product NDC	57237-240
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zaleplon
Non-Proprietary Name	Zaleplon
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20080606
Marketing Category Name	ANDA
Application Number	ANDA078829
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	ZALEPLON
Strength	10
Strength Unit	mg/1
Pharmacy Classes	Central Nervous System Depression [PE], GABA A Agonists [MoA], gamma-Aminobutyric Acid A Receptor Agonist [EPC]
DEA Schedule	CIV