Visitor Monitoring Drug Details: CARDIZEM
 
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Drug Details

Drug Name: CARDIZEM
FDA Application No: (NDA) 018602
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: BIOVAIL LABS INTL
Original Approval or Tentative Approval Date: November 5, 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
CARDIZEM DILTIAZEM HYDROCHLORIDE30MGTABLET; ORAL Prescription No AB
CARDIZEM DILTIAZEM HYDROCHLORIDE60MGTABLET; ORAL Prescription No AB
CARDIZEM DILTIAZEM HYDROCHLORIDE90MGTABLET; ORAL Prescription No AB
CARDIZEM DILTIAZEM HYDROCHLORIDE120MGTABLET; ORAL Prescription Yes AB


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