Visitor Monitoring Drug History: INTROPIN
 
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: INTROPIN
FDA Application No: (NDA) 017395
Active Ingredient(s): DOPAMINE HYDROCHLORIDE
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for INTROPIN, (NDA) 017395
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/5/2001 030Control Supplement  
6/17/1997 029Labeling Revision  
5/5/1995 028Labeling Revision  
10/7/1992 027Labeling Revision  
4/12/1990 026Manufacturing Change or Addition  
5/30/1986 025Manufacturing Change or Addition  
4/6/1983 024Package Change  
4/2/1982 023Formulation Revision  
2/8/1982 022Expiration Date Change  
9/15/1981 021Control Supplement  
7/23/1981 020Manufacturing Change or Addition  
11/12/1981 019Labeling Revision  
5/21/1981 018Labeling Revision  
9/15/1981 017Labeling Revision  
11/12/1981 016General Efficacy (MarkIV)  
11/14/1980 015Control Supplement  
1/14/1980 014Labeling Revision  
7/10/1980 013Formulation Revision  
7/10/1980 012Labeling Revision  
7/10/1980 011Control Supplement  
6/11/1979 010Labeling Revision  
6/11/1979 009Labeling Revision  
6/11/1979 008Labeling Revision  
8/24/1978 007Control Supplement  
10/6/1977 006Control Supplement  
1/20/1976 005Manufacturing Change or Addition  
5/3/1976 004Labeling Revision  
5/3/1976 003Labeling Revision  
10/7/1975 002Control Supplement  
4/30/1975 001Labeling Revision  
2/25/1974 000Approval  
 
Therapeutic Equivalents
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