Visitor Monitoring Drug Details: DILTIAZEM HYDROCHLORIDE
 
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Drug Details

Drug Name: DILTIAZEM HYDROCHLORIDE
FDA Application No: (ANDA) 074852
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: ANDRX
Original Approval or Tentative Approval Date: October 10, 1997
 
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
DILTIAZEM HYDROCHLORIDE DILTIAZEM HYDROCHLORIDE120MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB2
DILTIAZEM HYDROCHLORIDE DILTIAZEM HYDROCHLORIDE180MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB2
DILTIAZEM HYDROCHLORIDE DILTIAZEM HYDROCHLORIDE240MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB2


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