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Levetiracetam - 16729-066-16 - (levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 16729-066
Proprietary Name: Levetiracetam
Non Proprietary Name: levetiracetam
Active Ingredient(s): 750    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: 16729-066
Labeler Name: Accord Healthcare Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090843
Marketing Category: ANDA
Start Marketing Date: 20110314

Package Information of Levetiracetam

Package NDC: 16729-066-16
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (16729-066-16)

NDC Information of Levetiracetam

NDC Code 16729-066-16
Proprietary Name Levetiracetam
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (16729-066-16)
Product NDC 16729-066
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110314
Marketing Category Name ANDA
Labeler Name Accord Healthcare Inc.
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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