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Levetiracetam - 50268-468-15 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 50268-468
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
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 50268-468
Labeler Name: AvPAK
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077319
Marketing Category: ANDA
Start Marketing Date: 20090320

Package Information of Levetiracetam

Package NDC: 50268-468-15
Package Description: 50 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (50268-468-15)

NDC Information of Levetiracetam

NDC Code 50268-468-15
Proprietary Name Levetiracetam
Package Description 50 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (50268-468-15)
Product NDC 50268-468
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090320
Marketing Category Name ANDA
Labeler Name AvPAK
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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