Visitor Monitoring Drug Details: KADIAN
 
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Drug Details

Drug Name: KADIAN
FDA Application No: (NDA) 020616
Active Ingredient(s): MORPHINE SULFATE
Company: ALPHARMA PHARMS
Original Approval or Tentative Approval Date: July 3, 1996
Chemical Type: 3 New dosage form
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
KADIAN MORPHINE SULFATE20MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No None
KADIAN MORPHINE SULFATE50MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No None
KADIAN MORPHINE SULFATE100MGCAPSULE, EXTENDED RELEASE; ORAL Prescription Yes None
KADIAN MORPHINE SULFATE30MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No BX
KADIAN MORPHINE SULFATE60MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No BX
KADIAN MORPHINE SULFATE80MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No None
KADIAN MORPHINE SULFATE200MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No None
KADIAN MORPHINE SULFATE10MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No None


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