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Levetiracetam - 0093-7287-89 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 0093-7287
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
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 0093-7287
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078101
Marketing Category: ANDA
Start Marketing Date: 20090115

Package Information of Levetiracetam

Package NDC: 0093-7287-89
Package Description: 120 TABLET, FILM COATED in 1 BOTTLE (0093-7287-89)

NDC Information of Levetiracetam

NDC Code 0093-7287-89
Proprietary Name Levetiracetam
Package Description 120 TABLET, FILM COATED in 1 BOTTLE (0093-7287-89)
Product NDC 0093-7287
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090115
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


General Information