Visitor Monitoring Drug History: ISOPTIN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: ISOPTIN
FDA Application No: (NDA) 018593
Active Ingredient(s): VERAPAMIL HYDROCHLORIDE
Company: FSC
 
Label History
 
Labels are not available on this site for ISOPTIN, (NDA) 018593
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/14/1999 015Manufacturing Change or Addition  
7/20/1988 014Labeling Revision  
6/22/1988 013Manufacturing Change or Addition  
11/23/1987 012Manufacturing Change or Addition  
7/28/1987 011Control Supplement  
12/15/1988 010Control Supplement  
9/10/1984 008Manufacturing Change or Addition  
9/10/1984 007Package Change  
12/16/1986 006New or Modified Indication  
12/16/1986 004New or Modified Indication  
7/27/1982 001Package Change  
3/8/1982 000Approval  
 
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