Visitor Monitoring Drug History: GUANIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: GUANIDINE HYDROCHLORIDE
FDA Application No: (NDA) 001546
Active Ingredient(s): GUANIDINE HYDROCHLORIDE
Company: SCHERING
 
Label History
 
Labels are not available on this site for GUANIDINE HYDROCHLORIDE, (NDA) 001546
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/16/2000 015Manufacturing Change or Addition  
2/14/2000 014Manufacturing Change or Addition  
12/23/1998 013Manufacturing Change or Addition  
10/28/1992 012Manufacturing Change or Addition  
4/24/2002 011Labeling Revision Letter 
12/11/1986 010Control Supplement  
12/5/1984 009Manufacturing Change or Addition  
8/2/1983 008Package Change  
6/16/1980 007Manufacturing Change or Addition  
2/16/1978 006Manufacturing Change or Addition  
1/29/1975 004Control Supplement  
10/2/1939 000Approval  
 
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