Visitor Monitoring Drug History: RETIN-A
 
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: RETIN-A
FDA Application No: (NDA) 017955
Active Ingredient(s): TRETINOIN
Company: JOHNSON AND JOHNSON
 
Label History
 
View the label approved on June 10, 2002 for RETINA, (NDA) 017955


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
3/20/2001 024Package Change  
6/10/2002 023Labeling Revision Letter
Label 
1/25/1999 022Manufacturing Change or Addition  
7/23/1998 021Manufacturing Change or Addition  
6/10/2002 020Labeling Revision Letter
Label 
6/10/2002 019Labeling Revision Letter
Label 
1/24/1992 016Control Supplement  
7/3/1990 014Control Supplement  
8/28/1990 013Labeling Revision  
8/28/1990 012Labeling Revision  
12/1/1989 011Package Change  
6/11/1985 009Manufacturing Change or Addition  
7/23/1986 008Manufacturing Change or Addition  
6/6/1983 007Manufacturing Change or Addition  
7/29/1981 005Control Supplement  
12/6/1982 004Practioner Draft Labeling  
4/28/1980 003Distributor  
11/5/1979 002Control Supplement  
7/3/1979 001Manufacturing Change or Addition  
10/17/1978 000Approval  
 
Therapeutic Equivalents
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