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Levetiracetam - 55154-5699-0 - (levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 55154-5699
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: 55154-5699
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076919
Marketing Category: ANDA
Start Marketing Date: 20120829

Package Information of Levetiracetam

Package NDC: 55154-5699-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5699-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Levetiracetam

NDC Code 55154-5699-0
Proprietary Name Levetiracetam
Package Description 10 BLISTER PACK in 1 BAG (55154-5699-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5699
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120829
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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