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

Drug Name: LIDOCAINE HYDROCHLORIDE 0.4% IN DEXTROSE 5% IN PLASTIC CONTAINER
FDA Application No: (NDA) 018388
Active Ingredient(s): LIDOCAINE HYDROCHLORIDE
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for LIDOCAINE HYDROCHLORIDE 0.4 IN DEXTROSE 5 IN PLASTIC CONTAINER, (NDA) 018388
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/26/1999 067Labeling Revision  
11/5/1998 066Manufacturing Change or Addition  
6/12/1997 065Manufacturing Change or Addition  
8/26/1999 064Labeling Revision  
3/18/1997 063Control Supplement  
7/9/1996 062Package Change  
2/2/1996 061Package Change  
8/3/1995 060Manufacturing Change or Addition  
7/17/1996 059Control Supplement  
6/26/1996 058Control Supplement  
8/17/1995 056Package Change  
11/3/1993 055Labeling Revision  
8/30/1991 054Package Change  
1/28/1992 053Package Change  
9/10/1991 052Control Supplement  
1/11/1990 050Manufacturing Change or Addition  
2/22/1990 049Manufacturing Change or Addition  
5/1/1992 048Control Supplement  
11/26/1986 045Control Supplement  
8/8/1986 044Control Supplement  
6/10/1985 043Control Supplement  
5/10/1985 042Control Supplement  
12/15/1986 041Expiration Date Change  
1/31/1986 040Control Supplement  
10/26/1985 039Labeling Revision  
11/1/1985 038Labeling Revision  
5/3/1985 037Control Supplement  
10/26/1985 036Control Supplement  
11/1/1985 033Package Change  
10/22/1984 032Control Supplement  
9/26/1985 031Package Change  
10/29/1985 029Package Change  
11/28/1984 028Control Supplement  
9/13/1989 027Control Supplement  
4/9/1984 026Control Supplement  
10/17/1984 025Control Supplement  
3/21/1984 024Control Supplement  
9/6/1983 023Control Supplement  
6/16/1983 021Labeling Revision  
12/8/1983 020Control Supplement  
2/17/1984 019Control Supplement  
10/10/1984 018Labeling Revision  
10/10/1984 017Package Change  
7/26/1982 016Control Supplement  
3/1/1984 015Control Supplement  
2/15/1983 014Manufacturing Change or Addition  
7/8/1982 013Control Supplement  
11/5/1982 012Labeling Revision  
11/5/1982 011Control Supplement  
2/1/1982 010Control Supplement  
1/8/1982 009Control Supplement  
6/9/1982 007Control Supplement  
10/1/1981 006Labeling Revision  
4/21/1981 005Labeling Revision  
4/21/1981 004Control Supplement  
4/22/1981 003Labeling Revision  
5/16/1981 002Control Supplement  
12/19/1980 000Approval  
 
Therapeutic Equivalents
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