Visitor Monitoring Drug Details: DILT-CD
 
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Drug Details

Drug Name: DILT-CD
FDA Application No: (ANDA) 076151
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: TORPHARM
Original Approval or Tentative Approval Date: May 20, 2004
 
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
DILT-CD DILTIAZEM HYDROCHLORIDE120MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB3
DILT-CD DILTIAZEM HYDROCHLORIDE180MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB3
DILT-CD DILTIAZEM HYDROCHLORIDE240MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB3
DILT-CD DILTIAZEM HYDROCHLORIDE300MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB3


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