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LEVETIRACETAM - 16590-320-90 - (LEVETIRACETAM)

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Drug Information of LEVETIRACETAM

Product NDC: 16590-320
Proprietary Name: LEVETIRACETAM
Non Proprietary Name: LEVETIRACETAM
Active Ingredient(s): 250    mg/1 & nbsp;   LEVETIRACETAM
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LEVETIRACETAM

Product NDC: 16590-320
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078858
Marketing Category: ANDA
Start Marketing Date: 20090115

Package Information of LEVETIRACETAM

Package NDC: 16590-320-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (16590-320-90)

NDC Information of LEVETIRACETAM

NDC Code 16590-320-90
Proprietary Name LEVETIRACETAM
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (16590-320-90)
Product NDC 16590-320
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LEVETIRACETAM
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090115
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
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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