Visitor Monitoring Drug Details: PROCARDIA XL
 
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Drug Details

Drug Name: PROCARDIA XL
FDA Application No: (NDA) 019684
Active Ingredient(s): NIFEDIPINE
Company: PFIZER
Original Approval or Tentative Approval Date: September 6, 1989
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
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
PROCARDIA XL NIFEDIPINE30MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB2
PROCARDIA XL NIFEDIPINE60MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB2
PROCARDIA XL NIFEDIPINE90MGTABLET, EXTENDED RELEASE; ORAL Prescription Yes AB2


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