Visitor Monitoring Drug Details: BETIMOL
 
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Drug Details

Drug Name: BETIMOL
FDA Application No: (NDA) 020439
Active Ingredient(s): TIMOLOL
Company: SANTEN OY
Original Approval or Tentative Approval Date: March 31, 1995
Chemical Type: 2 New active ingredient
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
BETIMOL TIMOLOLEQ 0.25% BASESOLUTION/DROPS; OPHTHALMIC Prescription Yes None
BETIMOL TIMOLOLEQ 0.5% BASESOLUTION/DROPS; OPHTHALMIC Prescription Yes None


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