Visitor Monitoring Drug History: LIDOPEN
 
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: LIDOPEN
FDA Application No: (NDA) 017549
Active Ingredient(s): LIDOCAINE HYDROCHLORIDE
Company: MERIDIAN MEDCL TECHN
 
Label History
 
Labels are not available on this site for LIDOPEN, (NDA) 017549
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/31/2002 020Control Supplement  
10/20/2000 019Manufacturing Change or Addition  
12/8/1999 018Manufacturing Change or Addition  
7/21/1998 017Manufacturing Change or Addition  
4/18/1997 016Package Change  
1/9/1997 015Control Supplement  
6/6/1996 014Manufacturing Change or Addition  
5/10/1993 013Control Supplement  
12/23/1988 012Formulation Revision  
12/10/1986 011Labeling Revision  
4/16/1984 008Practioner Draft Labeling  
1/11/1978 007Labeling Revision  
3/17/1977 004Labeling Revision  
10/18/1976 003General Efficacy (MarkIV)  
12/4/1975 002Control Supplement  
9/24/1975 001Distributor  
3/28/1975 000Approval  
 
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