Visitor Monitoring Drug Details: VERELAN
 
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Drug Details

Drug Name: VERELAN
FDA Application No: (NDA) 019614
Active Ingredient(s): VERAPAMIL HYDROCHLORIDE
Company: ELAN DRUG
Original Approval or Tentative Approval Date: May 29, 1990
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
VERELAN VERAPAMIL HYDROCHLORIDE120MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB
VERELAN VERAPAMIL HYDROCHLORIDE240MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB
VERELAN VERAPAMIL HYDROCHLORIDE180MGCAPSULE, EXTENDED RELEASE; ORAL Prescription No AB
VERELAN VERAPAMIL HYDROCHLORIDE360MGCAPSULE, EXTENDED RELEASE; ORAL Prescription Yes None


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