"16571-788-50" National Drug Code (NDC)

NDC Code	16571-788-50
Package Description	500 TABLET, FILM COATED in 1 BOTTLE (16571-788-50)
Product NDC	16571-788
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Levetiracetam
Non-Proprietary Name	Levetiracetam
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20090115
End Marketing Date	20260331
Marketing Category Name	ANDA
Application Number	ANDA078993
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	LEVETIRACETAM
Strength	500
Strength Unit	mg/1
Pharmacy Classes	Decreased Central Nervous System Disorganized Electrical Activity [PE]