Visitor Monitoring Drug Details: KLONOPIN
 
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Drug Details

Drug Name: KLONOPIN
FDA Application No: (NDA) 017533
Active Ingredient(s): CLONAZEPAM
Company: ROCHE
Original Approval or Tentative Approval Date: June 4, 1975
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
Therapeutic Equivalents Labels are not available
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
KLONOPIN CLONAZEPAM0.5MGTABLET; ORAL Prescription No AB
KLONOPIN CLONAZEPAM1MGTABLET; ORAL Prescription Yes AB
KLONOPIN CLONAZEPAM2MGTABLET; ORAL Prescription No AB
KLONOPIN CLONAZEPAM0.125MGTABLET; ORAL Discontinued No None
KLONOPIN CLONAZEPAM0.25MGTABLET; ORAL Discontinued No None


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