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
 
 
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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