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Levetiracetam - 68180-114-09 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 68180-114
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: 68180-114
Labeler Name: Lupin Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078154
Marketing Category: ANDA
Start Marketing Date: 20090101

Package Information of Levetiracetam

Package NDC: 68180-114-09
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (68180-114-09)

NDC Information of Levetiracetam

NDC Code 68180-114-09
Proprietary Name Levetiracetam
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (68180-114-09)
Product NDC 68180-114
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 Lupin Pharmaceuticals, 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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