Visitor Monitoring Drug Details: CATAPRES
 
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Drug Details

Drug Name: CATAPRES
FDA Application No: (NDA) 017407
Active Ingredient(s): CLONIDINE HYDROCHLORIDE
Company: BOEHRINGER INGELHEIM
Original Approval or Tentative Approval Date: September 3, 1974
Chemical Type: 3 New dosage form
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
CATAPRES CLONIDINE HYDROCHLORIDE0.1MGTABLET; ORAL Prescription No AB
CATAPRES CLONIDINE HYDROCHLORIDE0.2MGTABLET; ORAL Prescription No AB
CATAPRES CLONIDINE HYDROCHLORIDE0.3MGTABLET; ORAL Prescription Yes AB


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