Visitor Monitoring Drug Details: DILTIAZEM HYDROCHLORIDE
 
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Drug Details

Drug Name: DILTIAZEM HYDROCHLORIDE
FDA Application No: (ANDA) 074910
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: MYLAN
Original Approval or Tentative Approval Date: May 2, 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 HYDROCHLORIDE60MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No None
DILTIAZEM HYDROCHLORIDE DILTIAZEM HYDROCHLORIDE90MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No None
DILTIAZEM HYDROCHLORIDE DILTIAZEM HYDROCHLORIDE120MGCAPSULE, EXTENDED RELEASE; ORAL Prescription Yes None


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