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) 000552
Active Ingredient(s): HEPARIN SODIUM
Company: ORGANON USA INC
 
Label History
 
Labels are not available on this site for HEPARIN SODIUM, (NDA) 000552
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/2/1990 024Manufacturing Change or Addition  
8/5/1988 023Labeling Revision  
12/9/1987 022Control Supplement  
1/6/1987 021Package Change  
7/28/1986 020Control Supplement  
4/11/1986 018New Dosage Regimen  
5/13/1985 017Practioner Draft Labeling  
11/28/1980 015Control Supplement  
11/28/1980 014Control Supplement  
3/24/1981 013Labeling Revision  
1/25/1978 012Labeling Revision  
6/8/1981 011Control Supplement  
5/15/1978 010Control Supplement  
7/28/1975 008Other Amendment  
7/28/1975 007Other Amendment  
2/9/1939 000Approval  
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test