Visitor Monitoring Drug Details: NALFON 200
 
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Drug Details

Drug Name: NALFON 200
FDA Application No: (NDA) 017604
Active Ingredient(s): FENOPROFEN CALCIUM
Company: PEDINOL
Original Approval or Tentative Approval Date: March 16, 1976
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority 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
NALFON FENOPROFEN CALCIUMEQ 300MG BASECAPSULE; ORAL Prescription Yes AB
NALFON 200 FENOPROFEN CALCIUMEQ 200MG BASECAPSULE; ORAL Prescription No AB


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