Visitor Monitoring Drug Details: CARTROL
 
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Drug Details

Drug Name: CARTROL
FDA Application No: (NDA) 019204
Active Ingredient(s): CARTEOLOL HYDROCHLORIDE
Company: ABBOTT
Original Approval or Tentative Approval Date: December 28, 1988
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no 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
CARTROL CARTEOLOL HYDROCHLORIDE2.5MGTABLET; ORAL Discontinued No None
CARTROL CARTEOLOL HYDROCHLORIDE5MGTABLET; ORAL Discontinued No None
CARTROL CARTEOLOL HYDROCHLORIDE10MGTABLET; ORAL Discontinued No None


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