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Levetiracetam - 0093-7796-06 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 0093-7796
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 750    mg/1 & nbsp;   Levetiracetam
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 0093-7796
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091430
Marketing Category: ANDA
Start Marketing Date: 20110913

Package Information of Levetiracetam

Package NDC: 0093-7796-06
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7796-06)

NDC Information of Levetiracetam

NDC Code 0093-7796-06
Proprietary Name Levetiracetam
Package Description 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7796-06)
Product NDC 0093-7796
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110913
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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