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Levetiracetam - 51991-649-36 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 51991-649
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 750    mg/1 & nbsp;   Levetiracetam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 51991-649
Labeler Name: Breckenridge Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090511
Marketing Category: ANDA
Start Marketing Date: 20111101

Package Information of Levetiracetam

Package NDC: 51991-649-36
Package Description: 120 TABLET in 1 BOTTLE (51991-649-36)

NDC Information of Levetiracetam

NDC Code 51991-649-36
Proprietary Name Levetiracetam
Package Description 120 TABLET in 1 BOTTLE (51991-649-36)
Product NDC 51991-649
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111101
Marketing Category Name ANDA
Labeler Name Breckenridge Pharmaceutical, Inc.
Substance Name LEVETIRACETAM
Strength Number 750
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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