Visitor Monitoring Drug History: ACETAMINOPHEN
 
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Label and Approval History

Drug Name: ACETAMINOPHEN
FDA Application No: (NDA) 018337
Active Ingredient(s): ACETAMINOPHEN
Company: ACTAVIS MID ATLANTIC
 
Label History
 
Labels are not available on this site for ACETAMINOPHEN, (NDA) 018337
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/9/2002 020Control Supplement  
9/21/2000 016Control Supplement  
6/15/1994 015Manufacturing Change or Addition  
8/26/1992 013Labeling Revision  
1/28/1993 012Control Supplement  
6/8/1988 008Labeling  
4/22/1980 000Approval  
 
Therapeutic Equivalents
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