Visitor Monitoring Drug Details: ZEMPLAR
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: ZEMPLAR
FDA Application No: (NDA) 021606
Active Ingredient(s): PARICALCITOL
Company: ABBOTT
Original Approval or Tentative Approval Date: May 26, 2005
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
ZEMPLAR PARICALCITOL1UGMCAPSULE; ORAL Prescription No None
ZEMPLAR PARICALCITOL2UGMCAPSULE; ORAL Prescription No None
ZEMPLAR PARICALCITOL4UGMCAPSULE; ORAL Prescription Yes None


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