Visitor Monitoring Drug History: ISOPROTERENOL HYDROCHLORIDE
 
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Label and Approval History

Drug Name: ISOPROTERENOL HYDROCHLORIDE
FDA Application No: (NDA) 010375
Active Ingredient(s): ISOPROTERENOL HYDROCHLORIDE
Company: 3M
 
Label History
 
Labels are not available on this site for ISOPROTERENOL HYDROCHLORIDE, (NDA) 010375
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/30/1997 023Labeling Revision  
12/20/1993 022Package Change  
12/15/1987 021Labeling Revision  
2/17/1987 020Practioner Draft Labeling  
3/5/1982 018Control Supplement  
9/18/1978 016Control Supplement  
4/13/1978 015Control Supplement  
11/9/1976 014Labeling Revision  
7/29/1975 013Control Supplement  
7/28/1975 008Control Supplement  
7/28/1975 007Control Supplement  
3/9/1956 000Approval  
 
Therapeutic Equivalents
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