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Levetiracetam - 49349-630-02 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 49349-630
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 250    mg/1 & nbsp;   Levetiracetam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 49349-630
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078858
Marketing Category: ANDA
Start Marketing Date: 20111207

Package Information of Levetiracetam

Package NDC: 49349-630-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-630-02)

NDC Information of Levetiracetam

NDC Code 49349-630-02
Proprietary Name Levetiracetam
Package Description 30 TABLET in 1 BLISTER PACK (49349-630-02)
Product NDC 49349-630
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111207
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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