Visitor Monitoring Drug Details: CAPOTEN
 
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Drug Details

Drug Name: CAPOTEN
FDA Application No: (NDA) 018343
Active Ingredient(s): CAPTOPRIL
Company: PAR PHARM
Original Approval or Tentative Approval Date: April 6, 1981
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
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
CAPOTEN CAPTOPRIL50MGTABLET; ORAL Prescription No AB
CAPOTEN CAPTOPRIL25MGTABLET; ORAL Prescription No AB
CAPOTEN CAPTOPRIL100MGTABLET; ORAL Prescription Yes AB
CAPOTEN CAPTOPRIL150MGTABLET; ORAL Discontinued No None
CAPOTEN CAPTOPRIL12.5MGTABLET; ORAL Prescription No AB
CAPOTEN CAPTOPRIL37.5MGTABLET; ORAL Discontinued No None
CAPOTEN CAPTOPRIL75MGTABLET; ORAL Discontinued No None


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