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Levetiracetam - 55111-182-05 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 55111-182
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 500    mg/1 & nbsp;   Levetiracetam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 55111-182
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076920
Marketing Category: ANDA
Start Marketing Date: 20090115

Package Information of Levetiracetam

Package NDC: 55111-182-05
Package Description: 500 TABLET in 1 BOTTLE (55111-182-05)

NDC Information of Levetiracetam

NDC Code 55111-182-05
Proprietary Name Levetiracetam
Package Description 500 TABLET in 1 BOTTLE (55111-182-05)
Product NDC 55111-182
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090115
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name LEVETIRACETAM
Strength Number 500
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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