Visitor Monitoring Drug History: HEMABATE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: HEMABATE
FDA Application No: (NDA) 017989
Active Ingredient(s): CARBOPROST TROMETHAMINE
Company: PHARMACIA AND UPJOHN
 
Label History
 
Labels are not available on this site for HEMABATE, (NDA) 017989
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/15/2002 014Control Supplement  
4/3/2000 013Manufacturing Change or Addition  
5/11/1998 012Labeling Revision  
8/29/1995 011Labeling Revision  
8/29/1995 010Labeling Revision  
5/8/1992 009Expiration Date Change  
9/3/1990 008Formulation Revision  
9/21/1988 007Labeling Revision  
9/8/1986 006Labeling Revision  
5/21/1985 005Labeling Revision  
8/30/1983 004Practioner Draft Labeling  
12/29/1981 003Labeling Revision  
3/20/1980 002Labeling Revision  
3/10/1981 001Labeling Revision  
1/9/1979 000Approval  
 
There are no Therapeutic Equivalents
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