Visitor Monitoring Drug History: LIDOCAINE HYDROCHLORIDE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER
 
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Label and Approval History

Drug Name: LIDOCAINE HYDROCHLORIDE 0.4% AND DEXTROSE 5% IN PLASTIC CONTAINER
FDA Application No: (NDA) 018461
Active Ingredient(s): LIDOCAINE HYDROCHLORIDE
Company: BAXTER HLTHCARE
 
Label History
 
View the label approved on January 23, 2002 for LIDOCAINE HYDROCHLORIDE 0.4 AND DEXTROSE 5 IN PLASTIC CONTAINER, (NDA) 018461


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
12/11/2003 052Labeling Revision Letter 
1/23/2002 050Labeling Revision Letter
Label
Review 
11/23/1999 048Package Change  
6/3/1999 047Manufacturing Change or Addition  
9/18/1998 046Labeling Revision  
9/29/1994 045Control Supplement  
3/16/1994 044Control Supplement  
1/8/1993 043Labeling Revision  
4/3/1991 041Control Supplement  
4/29/1991 040Control Supplement  
5/24/1990 039Control Supplement  
3/26/1991 038Control Supplement  
2/15/1991 037Control Supplement  
7/26/1989 036Control Supplement  
1/12/1989 035Control Supplement  
7/25/1987 033Package Change  
5/28/1987 032Control Supplement  
2/27/1986 028Package Change  
4/15/1985 027Control Supplement  
9/13/1985 026Labeling Revision  
6/13/1985 025Control Supplement  
10/23/1984 024Control Supplement  
9/4/1986 023Practioner Draft Labeling  
2/28/1984 022Control Supplement  
4/30/1984 021Labeling Revision  
6/11/1985 020Control Supplement  
3/14/1983 018Control Supplement  
1/24/1985 017Control Supplement  
3/16/1984 014Control Supplement  
5/25/1982 012Labeling Revision  
11/20/1981 011Control Supplement  
2/22/1982 009Labeling Revision  
2/22/1982 008Control Supplement  
6/3/1982 007Control Supplement  
10/1/1981 006Labeling Revision  
10/1/1981 005Control Supplement  
4/16/1982 004Control Supplement  
12/21/1981 003Control Supplement  
7/27/1981 002Labeling Revision  
7/22/1981 001Control Supplement  
4/22/1981 000Approval  
 
Therapeutic Equivalents
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