Visitor Monitoring Drug Details: NIFEDIPINE
 
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Drug Details

Drug Name: NIFEDIPINE
FDA Application No: (ANDA) 077899
Active Ingredient(s): NIFEDIPINE
Company: ABRIKA PHARMS
Original Approval or Tentative Approval Date: December 13, 2006
 
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
NIFEDIPINE NIFEDIPINE30MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB1
NIFEDIPINE NIFEDIPINE60MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB1


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