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Levetiracetam - 68180-117-07 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 68180-117
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 500    mg/1 & nbsp;   Levetiracetam
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 68180-117
Labeler Name: LUPIN PHARMACEUTICALS INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091399
Marketing Category: ANDA
Start Marketing Date: 20110912

Package Information of Levetiracetam

Package NDC: 68180-117-07
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-117-07)

NDC Information of Levetiracetam

NDC Code 68180-117-07
Proprietary Name Levetiracetam
Package Description 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-117-07)
Product NDC 68180-117
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110912
Marketing Category Name ANDA
Labeler Name LUPIN PHARMACEUTICALS INC
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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