Visitor Monitoring Drug Details: NEOPROFEN
 
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Drug Details

Drug Name: NEOPROFEN
FDA Application No: (NDA) 021903
Active Ingredient(s): IBUPROFEN LYSINE
Company: OVATION PHARMS
Original Approval or Tentative Approval Date: April 13, 2006
Chemical Type: 2 New active ingredient
Review Classification: P Priority review drug
O Orphan drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
NEOPROFEN IBUPROFEN LYSINEEQ 20MG BASE/2ML (EQ 10MG BASE/ML)INJECTABLE; INTRAVENOUS Prescription Yes None


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