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

Drug Name: REVIA
FDA Application No: (NDA) 018932
Active Ingredient(s): NALTREXONE HYDROCHLORIDE
Company: DURAMED
Original Approval or Tentative Approval Date: November 20, 1984
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
O Orphan 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
REVIA NALTREXONE HYDROCHLORIDE50MGTABLET; ORAL Prescription Yes AB


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