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Levetiracetam - 51672-4136-7 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 51672-4136
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 100    mg/mL & nbsp;   Levetiracetam
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 51672-4136
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078774
Marketing Category: ANDA
Start Marketing Date: 20090210

Package Information of Levetiracetam

Package NDC: 51672-4136-7
Package Description: 100 mL in 1 BOTTLE (51672-4136-7)

NDC Information of Levetiracetam

NDC Code 51672-4136-7
Proprietary Name Levetiracetam
Package Description 100 mL in 1 BOTTLE (51672-4136-7)
Product NDC 51672-4136
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20090210
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name LEVETIRACETAM
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Levetiracetam


General Information