Visitor Monitoring Drug History: FIORICET W/ CODEINE
 
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: FIORICET W/ CODEINE
FDA Application No: (NDA) 020232
Active Ingredient(s): ACETAMINOPHEN; BUTALBITAL; CAFFEINE; CODEINE PHOSPHATE
Company: WATSON PHARMS
 
Label History
 
Labels are not available on this site for FIORICET W CODEINE, (NDA) 020232
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/26/2002 016Control Supplement  
1/3/2002 015Control Supplement  
5/22/2001 014Manufacturing Change or Addition  
5/30/2001 013Control Supplement  
10/4/2001 012Labeling Revision  
8/3/1999 010Manufacturing Change or Addition  
4/22/1999 009Package Change  
5/20/1998 008Labeling Revision  
11/8/1995 005Manufacturing Change or Addition  
1/18/1996 004Labeling Revision  
3/29/1994 002Package Change  
12/1/1992 001Control Supplement  
7/30/1992 000Approval  
 
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