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Levetiracetam - 49884-204-02 - (levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 49884-204
Proprietary Name: Levetiracetam
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

Product NDC: 49884-204
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091291
Marketing Category: ANDA
Start Marketing Date: 20110913

Package Information of Levetiracetam

Package NDC: 49884-204-02
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-204-02)

NDC Information of Levetiracetam

NDC Code 49884-204-02
Proprietary Name Levetiracetam
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-204-02)
Product NDC 49884-204
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levetiracetam
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110913
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical 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 Levetiracetam


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