Visitor Monitoring Drug Details: TAZTIA XT
 
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Drug Details

Drug Name: TAZTIA XT
FDA Application No: (ANDA) 075401
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: ANDRX PHARMS
Original Approval or Tentative Approval Date: April 10, 2003
 
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
TAZTIA XT DILTIAZEM HYDROCHLORIDE120MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB4
TAZTIA XT DILTIAZEM HYDROCHLORIDE180MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB4
TAZTIA XT DILTIAZEM HYDROCHLORIDE240MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB4
TAZTIA XT DILTIAZEM HYDROCHLORIDE300MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB4
TAZTIA XT DILTIAZEM HYDROCHLORIDE360MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB4


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