Visitor Monitoring Drug Details: CARDIZEM LA
 
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Drug Details

Drug Name: CARDIZEM LA
FDA Application No: (NDA) 021392
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: BIOVAIL LABS INTL
Original Approval or Tentative Approval Date: February 6, 2003
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
CARDIZEM LA DILTIAZEM HYDROCHLORIDE120MGTABLET, EXTENDED RELEASE; ORAL Prescription No None
CARDIZEM LA DILTIAZEM HYDROCHLORIDE180MGTABLET, EXTENDED RELEASE; ORAL Prescription No None
CARDIZEM LA DILTIAZEM HYDROCHLORIDE240MGTABLET, EXTENDED RELEASE; ORAL Prescription No None
CARDIZEM LA DILTIAZEM HYDROCHLORIDE300MGTABLET, EXTENDED RELEASE; ORAL Prescription No None
CARDIZEM LA DILTIAZEM HYDROCHLORIDE360MGTABLET, EXTENDED RELEASE; ORAL Prescription No None
CARDIZEM LA DILTIAZEM HYDROCHLORIDE420MGTABLET, EXTENDED RELEASE; ORAL Prescription Yes None


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