Visitor Monitoring Drug History: DELFLEX W/ DEXTROSE 4.25% LOW MAGNESIUM IN PLASTIC CONTAINER
 
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Label and Approval History

Drug Name: DELFLEX W/ DEXTROSE 4.25% LOW MAGNESIUM IN PLASTIC CONTAINER
FDA Application No: (NDA) 018883
Active Ingredient(s): CALCIUM CHLORIDE; DEXTROSE; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Company: FRESENIUS MEDCL
 
Label History
 
Labels are not available on this site for DELFLEX W DEXTROSE 4.25 LOW MAGNESIUM IN PLASTIC CONTAINER, (NDA) 018883
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/26/2003 028Control Supplement Letter 
9/26/2001 026Package Change  
5/18/1999 025Package Change  
2/24/1997 024Control Supplement  
6/14/1996 023Control Supplement  
2/22/1996 022Control Supplement  
1/19/1996 021Control Supplement  
7/7/1993 020Manufacturing Change or Addition  
7/7/1993 019Labeling Revision  
7/7/1993 018Manufacturing Change or Addition  
7/11/1990 016Control Supplement  
1/10/1989 015Control Supplement  
2/5/1988 013Control Supplement  
1/24/1990 012Labeling Revision  
1/24/1990 011Control Supplement  
1/24/1990 010Labeling Revision  
1/24/1990 009Control Supplement  
4/8/1987 008Control Supplement  
1/14/1987 007Labeling Revision  
7/21/1987 006Control Supplement  
10/27/1987 005Labeling Revision  
10/27/1987 004Control Supplement  
6/16/1986 003Labeling Revision  
6/16/1986 002Manufacturing Change or Addition  
9/5/1985 001Expiration Date Change  
11/30/1984 000Approval  
 
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