Visitor Monitoring Drug Details: VERAPAMIL HYDROCHLORIDE
 
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Drug Details

Drug Name: VERAPAMIL HYDROCHLORIDE
FDA Application No: (ANDA) 075072
Active Ingredient(s): VERAPAMIL HYDROCHLORIDE
Company: KALI LABS
Original Approval or Tentative Approval Date: May 25, 1999
 
Therapeutic Equivalents Label Information
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
VERAPAMIL HYDROCHLORIDE VERAPAMIL HYDROCHLORIDE120MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB
VERAPAMIL HYDROCHLORIDE VERAPAMIL HYDROCHLORIDE240MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB


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