Visitor Monitoring Drug History: INDERIDE-40/25
 
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: INDERIDE-40/25
FDA Application No: (NDA) 018031
Active Ingredient(s): HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Company: WYETH PHARMS INC
 
Label History
 
Labels are not available on this site for INDERIDE4025, (NDA) 018031
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/21/2007 034Labeling Revision Letter 
12/29/2006 033Labeling Revision Letter 
6/9/2004 032Labeling Revision Letter 
5/3/2001 031Labeling Revision  
11/1/2001 030Labeling Revision  
11/7/1997 029Labeling Revision  
6/14/1994 028Manufacturing Change or Addition  
8/9/1989 027Package Change  
4/12/1989 026Package Change  
7/10/1989 025Control Supplement  
11/7/1988 024Labeling Revision  
5/25/1988 023Package Change  
12/30/1986 022Expiration Date Change  
10/8/1986 021Formulation Revision  
1/20/1987 021Package Change  
7/24/1986 019Control Supplement  
2/8/1990 018New Dosage Regimen  
2/8/1990 017Practioner Draft Labeling  
2/22/1985 016Manufacturing Change or Addition  
8/11/1983 015Control Supplement  
8/23/1982 013Formulation Revision  
6/9/1982 012Control Supplement  
4/28/1982 011Labeling Revision  
1/26/1982 010Manufacturing Change or Addition  
3/3/1982 009Manufacturing Change or Addition  
9/19/1980 008Formulation Revision  
4/12/1982 007Control Supplement  
1/27/1981 006Control Supplement  
10/3/1980 005Control Supplement  
3/27/1980 004Expiration Date Change  
5/28/1980 003Control Supplement  
12/10/1981 002Control Supplement  
7/31/1979 001Package Change  
6/15/1979 000Approval  
 
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