Visitor Monitoring Drug History: HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
 
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Label and Approval History

Drug Name: HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No: (NDA) 019042
Active Ingredient(s): HEPARIN SODIUM
Company: B BRAUN
 
Label History
 
Labels are not available on this site for HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (NDA) 019042
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/20/1992 006Manufacturing Change or Addition  
3/30/1990 005Package Change  
6/21/1989 004Labeling Revision  
4/17/1987 002Control Supplement  
9/10/1985 001Package Change  
3/29/1985 000Approval  
 
Therapeutic Equivalents
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