Visitor Monitoring Drug History: LENTE
 
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: LENTE
FDA Application No: (NDA) 018383
Active Ingredient(s): INSULIN ZINC SUSP PURIFIED PORK
Company: NOVO NORDISK INC
 
Label History
 
Labels are not available on this site for LENTE, (NDA) 018383
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/16/1997 025Labeling Revision Review 
4/10/1997 024Labeling Revision  
3/8/1995 023Control Supplement  
3/8/1995 022Control Supplement  
3/8/1995 021Package Change  
3/8/1995 020Package Change  
1/3/1994 019Labeling Revision  
1/3/1994 018Labeling Revision  
1/7/1994 017Labeling Revision  
12/7/1992 016Control Supplement  
7/28/1992 015Control Supplement  
3/18/1992 014Control Supplement  
9/19/1991 013Control Supplement  
2/16/1990 012Control Supplement  
2/27/1989 010Control Supplement  
9/17/1986 009Labeling Revision  
8/28/1985 008Control Supplement  
5/8/1985 007Labeling Revision  
6/14/1984 006Control Supplement  
8/10/1984 004Labeling Revision  
9/26/1983 003Labeling Revision  
10/23/1981 001Control Supplement  
3/17/1980 000Approval  
 
Therapeutic Equivalents
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