Home > National Drug Code (NDC) > levetiracetam extended-release

levetiracetam extended-release - 60505-3280-6 - (levetiracetam)

Alphabetical Index


Drug Information of levetiracetam extended-release

Product NDC: 60505-3280
Proprietary Name: levetiracetam extended-release
Non Proprietary Name: levetiracetam
Active Ingredient(s): 500    mg/1 & nbsp;   levetiracetam
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of levetiracetam extended-release

Product NDC: 60505-3280
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091261
Marketing Category: ANDA
Start Marketing Date: 20110912

Package Information of levetiracetam extended-release

Package NDC: 60505-3280-6
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-3280-6)

NDC Information of levetiracetam extended-release

NDC Code 60505-3280-6
Proprietary Name levetiracetam extended-release
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (60505-3280-6)
Product NDC 60505-3280
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levetiracetam
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110912
Marketing Category Name ANDA
Labeler Name Apotex Corp.
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 extended-release


General Information