Visitor Monitoring Drug History: URISPAS
 
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: URISPAS
FDA Application No: (NDA) 016769
Active Ingredient(s): FLAVOXATE HYDROCHLORIDE
Company: ORTHO MCNEIL PHARM
 
Label History
 
Labels are not available on this site for URISPAS, (NDA) 016769
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/3/2001 033Manufacturing Change or Addition  
4/21/2000 032Manufacturing Change or Addition  
10/29/1999 031Control Supplement  
3/19/1996 030Control Supplement  
9/27/1994 029Control Supplement  
1/4/1984 027Control Supplement  
10/8/1982 026Labeling Revision  
9/18/1985 025Practioner Draft Labeling  
5/29/1979 024Labeling Revision  
1/4/1979 023Labeling Revision  
5/15/1978 022Expiration Date Change  
5/15/1978 021Control Supplement  
7/13/1977 020Labeling Revision  
7/13/1977 019Labeling Revision  
4/27/1977 018Expiration Date Change  
9/24/1976 017Labeling Revision  
9/24/1976 016Labeling Revision  
8/10/1976 014Control Supplement  
6/18/1976 013Labeling Revision  
4/19/1976 012Labeling Revision  
1/9/1976 011Control Supplement  
7/25/1975 010Control Supplement  
1/15/1970 000Approval  
 
Therapeutic Equivalents
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