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Levetiracetam - 13668-016-25 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 13668-016
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 750    mg/1 & nbsp;   Levetiracetam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 13668-016
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078858
Marketing Category: ANDA
Start Marketing Date: 20090115

Package Information of Levetiracetam

Package NDC: 13668-016-25
Package Description: 250 TABLET in 1 BOTTLE (13668-016-25)

NDC Information of Levetiracetam

NDC Code 13668-016-25
Proprietary Name Levetiracetam
Package Description 250 TABLET in 1 BOTTLE (13668-016-25)
Product NDC 13668-016
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 Torrent Pharmaceuticals Limited
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


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