Visitor Monitoring Drug History: REGITINE
 
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: REGITINE
FDA Application No: (NDA) 008278
Active Ingredient(s): PHENTOLAMINE MESYLATE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for REGITINE, (NDA) 008278
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/29/1999 020Manufacturing Change or Addition  
2/5/1999 019Manufacturing Change or Addition  
11/5/1998 018Manufacturing Change or Addition  
10/20/1998 017Manufacturing Change or Addition  
1/9/1992 016Control Supplement  
4/14/1986 015Control Supplement  
7/21/1983 013Package Change  
7/27/1983 012Manufacturing Change or Addition  
5/13/1985 011Practioner Draft Labeling  
9/9/1981 010Expiration Date Change  
2/18/1981 009Package Change  
1/7/1980 008Package Change  
2/11/1977 007Expiration Date Change  
4/12/1977 006Labeling Revision  
2/11/1977 005Formulation Revision  
1/30/1952 000Approval  
 
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