Visitor Monitoring Drug Details: ISOPTIN
 
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Drug Details

Drug Name: ISOPTIN
FDA Application No: (NDA) 018593
Active Ingredient(s): VERAPAMIL HYDROCHLORIDE
Company: FSC
Original Approval or Tentative Approval Date: March 8, 1982
Chemical Type: 3 New dosage form
Review Classification: P Priority 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
ISOPTIN VERAPAMIL HYDROCHLORIDE80MGTABLET; ORAL Discontinued No None
ISOPTIN VERAPAMIL HYDROCHLORIDE120MGTABLET; ORAL Discontinued No None
ISOPTIN VERAPAMIL HYDROCHLORIDE40MGTABLET; ORAL Discontinued No None


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