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

Drug Name: NAPROSYN
FDA Application No: (NDA) 017581
Active Ingredient(s): NAPROXEN
Company: ROCHE PALO
Original Approval or Tentative Approval Date: March 11, 1976
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
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
NAPROSYN NAPROXEN250MGTABLET; ORAL Prescription No AB
NAPROSYN NAPROXEN375MGTABLET; ORAL Prescription No AB
NAPROSYN NAPROXEN500MGTABLET; ORAL Prescription Yes AB


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