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Levetiracetam - 31722-538-12 - (Levetiracetam)

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Drug Information of Levetiracetam

Product NDC: 31722-538
Proprietary Name: Levetiracetam
Non Proprietary Name: Levetiracetam
Active Ingredient(s): 750    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: 31722-538
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090515
Marketing Category: ANDA
Start Marketing Date: 20120109

Package Information of Levetiracetam

Package NDC: 31722-538-12
Package Description: 12 BOTTLE in 1 CASE (31722-538-12) > 120 TABLET, FILM COATED in 1 BOTTLE

NDC Information of Levetiracetam

NDC Code 31722-538-12
Proprietary Name Levetiracetam
Package Description 12 BOTTLE in 1 CASE (31722-538-12) > 120 TABLET, FILM COATED in 1 BOTTLE
Product NDC 31722-538
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levetiracetam
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120109
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
Substance Name LEVETIRACETAM
Strength Number 750
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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