Visitor Monitoring Drug Details: TIAZAC
 
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Drug Details

Drug Name: TIAZAC
FDA Application No: (NDA) 020401
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: BIOVAIL
Original Approval or Tentative Approval Date: September 11, 1995
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
TIAZAC DILTIAZEM HYDROCHLORIDE120MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB4
TIAZAC DILTIAZEM HYDROCHLORIDE180MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB4
TIAZAC DILTIAZEM HYDROCHLORIDE240MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB4
TIAZAC DILTIAZEM HYDROCHLORIDE300MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB4
TIAZAC DILTIAZEM HYDROCHLORIDE360MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB4
TIAZAC DILTIAZEM HYDROCHLORIDE420MGCAPSULE, EXTENDED RELEASE; ORAL Prescription Yes AB4


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