KEPPRA - 16590-135-30 - (LEVETIRACETAM)

Alphabetical Index


Drug Information of KEPPRA

Product NDC: 16590-135
Proprietary Name: KEPPRA
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 KEPPRA

Product NDC: 16590-135
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021035
Marketing Category: NDA
Start Marketing Date: 20000424

Package Information of KEPPRA

Package NDC: 16590-135-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16590-135-30)

NDC Information of KEPPRA

NDC Code 16590-135-30
Proprietary Name KEPPRA
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16590-135-30)
Product NDC 16590-135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LEVETIRACETAM
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20000424
Marketing Category Name NDA
Labeler Name STAT RX USA LLC
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 KEPPRA


General Information