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) 017340
Active Ingredient(s): TRETINOIN
Company: JOHNSON AND JOHNSON
 
Label History
 
View the label approved on June 10, 2002 for RETINA, (NDA) 017340


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
12/6/2002 038Manufacturing Change or Addition  
3/20/2001 037Package Change  
6/10/2002 036Labeling Revision Letter
Label 
1/25/1999 035Manufacturing Change or Addition  
7/23/1998 034Manufacturing Change or Addition  
6/10/2002 033Labeling Revision Letter
Label 
6/10/2002 032Labeling Revision Letter
Label 
1/24/1992 030Control Supplement  
7/3/1990 029Control Supplement  
8/28/1990 028Labeling Revision  
8/28/1990 027Labeling Revision  
12/1/1989 026Package Change  
4/12/1989 025Labeling Revision  
8/26/1986 023Package Change  
6/11/1985 022Manufacturing Change or Addition  
7/24/1986 021Manufacturing Change or Addition  
3/30/1984 020Control Supplement  
6/6/1983 019Manufacturing Change or Addition  
7/28/1981 018Control Supplement  
12/13/1982 017Distributor  
12/4/1978 015Labeling Revision  
1/4/1977 014Distributor  
6/30/1976 013Manufacturing Change or Addition  
8/27/1974 010Control Supplement  
4/15/1974 009Supplement  
4/15/1974 007Supplement  
1/26/1973 000Approval  
 
Therapeutic Equivalents
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