Keppra - 50474-597-66 - (levetiracetam)

Alphabetical Index


Drug Information of Keppra

Product NDC: 50474-597
Proprietary Name: Keppra
Non Proprietary Name: levetiracetam
Active Ingredient(s): 1000    mg/1 & nbsp;   levetiracetam
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Keppra

Product NDC: 50474-597
Labeler Name: UCB, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021035
Marketing Category: NDA
Start Marketing Date: 20000424

Package Information of Keppra

Package NDC: 50474-597-66
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50474-597-66)

NDC Information of Keppra

NDC Code 50474-597-66
Proprietary Name Keppra
Package Description 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50474-597-66)
Product NDC 50474-597
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000424
Marketing Category Name NDA
Labeler Name UCB, Inc.
Substance Name LEVETIRACETAM
Strength Number 1000
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Keppra


General Information