Visitor Monitoring Drug Details: KEPPRA
 
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Drug Details

Drug Name: KEPPRA
FDA Application No: (NDA) 021035
Active Ingredient(s): LEVETIRACETAM
Company: UCB INC
Original Approval or Tentative Approval Date: November 30, 1999
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
KEPPRA LEVETIRACETAM250MGTABLET; ORAL Prescription No None
KEPPRA LEVETIRACETAM500MGTABLET; ORAL Prescription No None
KEPPRA LEVETIRACETAM750MGTABLET; ORAL Prescription No None
KEPPRA LEVETIRACETAM1GMTABLET; ORAL Prescription Yes None


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