Visitor Monitoring Drug Details: BETAXOLOL HYDROCHLORIDE
 
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Drug Details

Drug Name: BETAXOLOL HYDROCHLORIDE
FDA Application No: (ANDA) 075541
Active Ingredient(s): BETAXOLOL HYDROCHLORIDE
Company: ACTAVIS TOTOWA
Original Approval or Tentative Approval Date: October 22, 1999
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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
BETAXOLOL HYDROCHLORIDE BETAXOLOL HYDROCHLORIDE10MGTABLET; ORAL Prescription No AB
BETAXOLOL HYDROCHLORIDE BETAXOLOL HYDROCHLORIDE20MGTABLET; ORAL Prescription No AB


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