Visitor Monitoring Drug Details: CARDURA
 
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Drug Details

Drug Name: CARDURA
FDA Application No: (NDA) 019668
Active Ingredient(s): DOXAZOSIN MESYLATE
Company: PFIZER
Original Approval or Tentative Approval Date: November 2, 1990
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard 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
CARDURA DOXAZOSIN MESYLATEEQ 1MG BASETABLET; ORAL Prescription Yes AB
CARDURA DOXAZOSIN MESYLATEEQ 2MG BASETABLET; ORAL Prescription No AB
CARDURA DOXAZOSIN MESYLATEEQ 4MG BASETABLET; ORAL Prescription No AB
CARDURA DOXAZOSIN MESYLATEEQ 8MG BASETABLET; ORAL Prescription No AB


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