Visitor Monitoring Drug History: INDERIDE LA 120/50
 
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Label and Approval History

Drug Name: INDERIDE LA 120/50
FDA Application No: (NDA) 019059
Active Ingredient(s): HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Company: WYETH AYERST
 
Label History
 
Labels are not available on this site for INDERIDE LA 12050, (NDA) 019059
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/3/2001 017Labeling Revision  
11/1/2001 016Labeling Revision  
5/8/1998 015Labeling Revision  
5/14/1990 014Expiration Date Change  
4/12/1989 013Package Change  
4/10/1989 012Control Supplement  
1/25/1989 011Control Supplement  
5/25/1988 010Package Change  
1/6/1987 009Expiration Date Change  
11/12/1986 008Manufacturing Change or Addition  
1/20/1987 007Formulation Revision  
7/2/1986 005Manufacturing Change or Addition  
3/20/1986 004Control Supplement  
3/20/1986 003Expiration Date Change  
7/24/1986 002Manufacturing Change or Addition  
10/22/1985 001Formulation Revision  
7/3/1985 000Approval  
 
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