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Levetiracetam - 63739-539-50 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 63739-539
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: 63739-539
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079107
Marketing Category: ANDA
Start Marketing Date: 20111101

Package Information of Levetiracetam

Package NDC: 63739-539-50
Package Description: 2 TRAY in 1 CASE (63739-539-50) > 20 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE

NDC Information of Levetiracetam

NDC Code 63739-539-50
Proprietary Name Levetiracetam
Package Description 2 TRAY in 1 CASE (63739-539-50) > 20 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE
Product NDC 63739-539
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20111101
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
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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