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) 017522
Active Ingredient(s): TRETINOIN
Company: JOHNSON AND JOHNSON
 
Label History
 
View the label approved on June 10, 2002 for RETINA, (NDA) 017522


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 028Manufacturing Change or Addition  
3/20/2001 027Package Change  
6/10/2002 026Labeling Revision Letter
Label 
1/25/1999 025Manufacturing Change or Addition  
7/23/1998 024Manufacturing Change or Addition  
6/10/2002 023Labeling Revision Letter
Label 
6/10/2002 022Labeling Revision Letter
Label 
1/24/1992 020Control Supplement  
7/3/1990 019Control Supplement  
8/28/1990 018Labeling Revision  
8/28/1990 017Labeling Revision  
12/1/1989 016Package Change  
8/26/1986 014Package Change  
6/17/1985 013Manufacturing Change or Addition  
7/23/1986 012Manufacturing Change or Addition  
4/2/1984 011Control Supplement  
6/6/1983 010Manufacturing Change or Addition  
7/29/1981 009Control Supplement  
12/3/1982 008Practioner Draft Labeling  
4/28/1980 007Distributor  
12/1/1978 005Labeling Revision  
4/19/1978 004Package Change  
1/4/1977 003Distributor  
6/29/1976 002Manufacturing Change or Addition  
10/24/1974 001Control Supplement  
7/19/1974 000Approval  
 
Therapeutic Equivalents
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