Visitor Monitoring Drug History: NORMODYNE
 
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: NORMODYNE
FDA Application No: (NDA) 018686
Active Ingredient(s): LABETALOL HYDROCHLORIDE
Company: SCHERING
 
Label History
 
Labels are not available on this site for NORMODYNE, (NDA) 018686
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/6/2001 029Control Supplement  
6/5/2001 028Manufacturing Change or Addition  
11/16/2000 027Manufacturing Change or Addition  
4/25/2000 026Labeling Revision  
8/10/1999 025Manufacturing Change or Addition  
4/29/1999 024Control Supplement  
11/14/1997 023Manufacturing Change or Addition  
7/9/1997 022Manufacturing Change or Addition  
11/25/1996 021Labeling Revision  
11/7/1996 020Manufacturing Change or Addition  
1/12/1995 019Labeling Revision  
5/28/1993 018Control Supplement  
9/16/1991 017Control Supplement  
10/15/1992 016Labeling Revision  
11/7/1990 015Labeling Revision  
10/19/1989 013Labeling Revision  
7/21/1989 012Package Change  
11/22/1988 011Control Supplement  
10/19/1989 010Labeling Revision  
4/14/1988 009Labeling Revision  
6/12/1987 008Manufacturing Change or Addition  
2/5/1987 007Manufacturing Change or Addition  
8/31/1987 006Labeling Revision  
8/31/1987 005Labeling Revision  
8/29/1986 004Package Change  
8/8/1986 003Control Supplement  
1/14/1986 002Control Supplement  
4/4/1986 001Package Change  
8/1/1984 000Approval  
 
Therapeutic Equivalents
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