Visitor Monitoring Drug Details: NAPRELAN
 
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Drug Details

Drug Name: NAPRELAN
FDA Application No: (NDA) 020353
Active Ingredient(s): NAPROXEN SODIUM
Company: STAT TRADE
Original Approval or Tentative Approval Date: January 5, 1996
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
 
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
NAPRELAN NAPROXEN SODIUMEQ 375MG BASETABLET, EXTENDED RELEASE; ORAL Prescription Yes AB
NAPRELAN NAPROXEN SODIUMEQ 500MG BASETABLET, EXTENDED RELEASE; ORAL Prescription Yes AB
NAPRELAN NAPROXEN SODIUMEQ 750MG BASETABLET, EXTENDED RELEASE; ORAL Discontinued No None


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