Visitor Monitoring Drug Details: PATANOL
 
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Drug Details

Drug Name: PATANOL
FDA Application No: (NDA) 020688
Active Ingredient(s): OLOPATADINE HYDROCHLORIDE
Company: ALCON
Original Approval or Tentative Approval Date: December 18, 1996
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
PATANOL OLOPATADINE HYDROCHLORIDEEQ 0.1% BASESOLUTION/DROPS; OPHTHALMIC Prescription Yes None


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