Visitor Monitoring Drug Details: NICARDIPINE HYDROCHLORIDE
 
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Drug Details

Drug Name: NICARDIPINE HYDROCHLORIDE
FDA Application No: (ANDA) 074642
Active Ingredient(s): NICARDIPINE HYDROCHLORIDE
Company: MYLAN
Original Approval or Tentative Approval Date: July 18, 1996
 
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
NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE20MGCAPSULE; ORAL Prescription No AB
NICARDIPINE HYDROCHLORIDE NICARDIPINE HYDROCHLORIDE30MGCAPSULE; ORAL Prescription No AB


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