Visitor Monitoring Drug History: PHENERGAN
 
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: PHENERGAN
FDA Application No: (NDA) 010926
Active Ingredient(s): PROMETHAZINE HYDROCHLORIDE
Company: WYETH PHARMS INC
 
Label History
 
View the label approved on November 15, 2004 for PHENERGAN, (NDA) 010926


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/8/2004 030Labeling Revision Letter
Label 
9/12/2001 027Control Supplement  
12/26/2002 022Labeling Revision Letter 
12/26/2002 021Labeling Revision Letter 
12/26/2002 020Labeling Revision Letter 
7/27/2001 019Manufacturing Change or Addition  
6/22/2001 018Manufacturing Change or Addition  
12/26/2002 017Labeling Revision Letter 
7/1/1994 016Control Supplement  
3/30/1992 015Manufacturing Change or Addition  
4/28/1993 014Manufacturing Change or Addition  
6/30/1988 011Control Supplement  
1/22/1988 010Labeling Revision  
5/29/1986 007Control Supplement  
5/5/1958 000Approval  
 
There are no Therapeutic Equivalents
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