Visitor Monitoring Drug Details: VASCOR
 
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Drug Details

Drug Name: VASCOR
FDA Application No: (NDA) 019002
Active Ingredient(s): BEPRIDIL HYDROCHLORIDE
Company: JOHNSON AND JOHNSON
Original Approval or Tentative Approval Date: December 28, 1990
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
VASCOR BEPRIDIL HYDROCHLORIDE200MGTABLET; ORAL Discontinued No None
VASCOR BEPRIDIL HYDROCHLORIDE300MGTABLET; ORAL Discontinued No None
VASCOR BEPRIDIL HYDROCHLORIDE400MGTABLET; ORAL Discontinued No None


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