Visitor Monitoring Drug Details: DILTIAZEM HYDROCHLORIDE
 
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Drug Details

Drug Name: DILTIAZEM HYDROCHLORIDE
FDA Application No: (ANDA) 074894
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: TEVA PARENTERAL
Original Approval or Tentative Approval Date: August 26, 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 HYDROCHLORIDE5MG/MLINJECTABLE; INJECTION Prescription No AP
DILTIAZEM HYDROCHLORIDE DILTIAZEM HYDROCHLORIDE10MG/MLINJECTABLE; INJECTION Prescription Yes None


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