Visitor Monitoring Drug Details: CARTIA XT
 
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Drug Details

Drug Name: CARTIA XT
FDA Application No: (ANDA) 074752
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: ANDRX PHARMS
Original Approval or Tentative Approval Date: July 9, 1998
 
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
CARTIA XT DILTIAZEM HYDROCHLORIDE180MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB3
CARTIA XT DILTIAZEM HYDROCHLORIDE120MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB3
CARTIA XT DILTIAZEM HYDROCHLORIDE240MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB3
CARTIA XT DILTIAZEM HYDROCHLORIDE300MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB3


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