Visitor Monitoring Drug Details: OMNARIS
 
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Drug Details

Drug Name: OMNARIS
FDA Application No: (NDA) 022004
Active Ingredient(s): CICLESONIDE
Company: ALTANA PHARMA
Original Approval or Tentative Approval Date: October 20, 2006
Chemical Type: 1 New molecular entity (NME)
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
OMNARIS CICLESONIDE0.05MG/INHSPRAY, METERED; NASAL Prescription Yes None


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