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Levetiracetam - 35356-429-60 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 35356-429
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 250    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: 35356-429
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078154
Marketing Category: ANDA
Start Marketing Date: 20120123

Package Information of Levetiracetam

Package NDC: 35356-429-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (35356-429-60)

NDC Information of Levetiracetam

NDC Code 35356-429-60
Proprietary Name Levetiracetam
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (35356-429-60)
Product NDC 35356-429
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120123
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name LEVETIRACETAM
Strength Number 250
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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