Home > National Drug Code (NDC) > Levetiracetam

Levetiracetam - 0228-4417-06 - (Levetiracetam)

Alphabetical Index


Drug Information of Levetiracetam

Product NDC: 0228-4417
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 500    mg/1 & nbsp;   Levetiracetam
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 0228-4417
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091557
Marketing Category: ANDA
Start Marketing Date: 20110912

Package Information of Levetiracetam

Package NDC: 0228-4417-06
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-4417-06)

NDC Information of Levetiracetam

NDC Code 0228-4417-06
Proprietary Name Levetiracetam
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-4417-06)
Product NDC 0228-4417
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110912
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
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 Levetiracetam


General Information