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Levetiracetam - 65862-250-47 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 65862-250
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 100    mg/mL & nbsp;   Levetiracetam
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Levetiracetam

Product NDC: 65862-250
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079063
Marketing Category: ANDA
Start Marketing Date: 20090115

Package Information of Levetiracetam

Package NDC: 65862-250-47
Package Description: 473 mL in 1 BOTTLE, PLASTIC (65862-250-47)

NDC Information of Levetiracetam

NDC Code 65862-250-47
Proprietary Name Levetiracetam
Package Description 473 mL in 1 BOTTLE, PLASTIC (65862-250-47)
Product NDC 65862-250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20090115
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name LEVETIRACETAM
Strength Number 100
Strength Unit mg/mL
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Levetiracetam


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