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Levetiracetam - 65977-5036-3 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 65977-5036
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: 65977-5036
Labeler Name: Hetero Drugs Ltd.,
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090515
Marketing Category: ANDA
Start Marketing Date: 20101008

Package Information of Levetiracetam

Package NDC: 65977-5036-3
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (65977-5036-3)

NDC Information of Levetiracetam

NDC Code 65977-5036-3
Proprietary Name Levetiracetam
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (65977-5036-3)
Product NDC 65977-5036
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101008
Marketing Category Name ANDA
Labeler Name Hetero Drugs Ltd.,
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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