Keppra - 54868-4947-2 - (levetiracetam)

Alphabetical Index


Drug Information of Keppra

Product NDC: 54868-4947
Proprietary Name: Keppra
Non Proprietary Name: levetiracetam
Active Ingredient(s): 500    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: 54868-4947
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021035
Marketing Category: NDA
Start Marketing Date: 20031030

Package Information of Keppra

Package NDC: 54868-4947-2
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4947-2)

NDC Information of Keppra

NDC Code 54868-4947-2
Proprietary Name Keppra
Package Description 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-4947-2)
Product NDC 54868-4947
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20031030
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name LEVETIRACETAM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Keppra


General Information