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Levetiracetam - 50436-5604-2 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 50436-5604
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: 50436-5604
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078154
Marketing Category: ANDA
Start Marketing Date: 20090101

Package Information of Levetiracetam

Package NDC: 50436-5604-2
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (50436-5604-2)

NDC Information of Levetiracetam

NDC Code 50436-5604-2
Proprietary Name Levetiracetam
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (50436-5604-2)
Product NDC 50436-5604
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090101
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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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