Visitor Monitoring Drug Details: WYTENSIN
 
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Drug Details

Drug Name: WYTENSIN
FDA Application No: (NDA) 018587
Active Ingredient(s): GUANABENZ ACETATE
Company: WYETH AYERST
Original Approval or Tentative Approval Date: September 7, 1982
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
WYTENSIN GUANABENZ ACETATEEQ 4MG BASETABLET; ORAL Discontinued No None
WYTENSIN GUANABENZ ACETATEEQ 8MG BASETABLET; ORAL Discontinued No None
WYTENSIN GUANABENZ ACETATEEQ 16MG BASETABLET; ORAL Discontinued No None


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