Visitor Monitoring Drug History: HEPARIN SODIUM
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: HEPARIN SODIUM
FDA Application No: (NDA) 017979
Active Ingredient(s): HEPARIN SODIUM
Company: ABRAXIS PHARM
 
Label History
 
Labels are not available on this site for HEPARIN SODIUM, (NDA) 017979
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/6/2003 029Manufacturing Change or Addition  
9/28/2001 028Control Supplement  
12/13/1999 026Manufacturing Change or Addition  
12/22/1997 025Manufacturing Change or Addition  
6/2/1995 024Control Supplement  
8/26/1993 021Labeling Revision  
2/9/1989 018Labeling Revision  
10/19/1988 016Labeling Revision  
9/17/1986 015Control Supplement  
7/29/1985 014Labeling Revision  
1/8/1985 013Manufacturing Change or Addition  
9/19/1984 012Manufacturing Change or Addition  
12/19/1983 011General Efficacy (MarkIV)  
1/12/1983 010Manufacturing Change or Addition  
9/23/1980 009Formulation Revision  
10/19/1979 007Control Supplement  
10/10/1979 006Control Supplement  
10/19/1979 005Formulation Revision  
9/18/1979 004Control Supplement  
10/3/1979 003Control Supplement  
5/29/1979 002Control Supplement  
3/29/1979 001Control Supplement  
12/21/1978 000Approval  
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test