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Levetiracetam - 24236-921-21 - (levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 24236-921
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: 24236-921
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076919
Marketing Category: ANDA
Start Marketing Date: 20130318

Package Information of Levetiracetam

Package NDC: 24236-921-21
Package Description: 120 TABLET, FILM COATED in 1 CANISTER (24236-921-21)

NDC Information of Levetiracetam

NDC Code 24236-921-21
Proprietary Name Levetiracetam
Package Description 120 TABLET, FILM COATED in 1 CANISTER (24236-921-21)
Product NDC 24236-921
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130318
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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