Visitor Monitoring Drug History: CLONIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CLONIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 070976
Active Ingredient(s): CLONIDINE HYDROCHLORIDE
Company: ACTAVIS ELIZABETH
 
Label History
 
Labels are not available on this site for CLONIDINE HYDROCHLORIDE, (ANDA) 070976
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/8/2002 015Control Supplement  
11/2/2001 014Control Supplement  
3/20/2000 013Facility Addition  
3/20/2000 012Facility Addition  
10/21/1999 011Chemistry  
2/18/1997 010Labeling  
1/18/1996 008Chemistry  
2/4/1992 007Chemistry  
10/13/1989 006Labeling  
11/17/1988 005Labeling  
5/10/1988 004Labeling  
1/28/1988 003Chemistry  
1/28/1988 002Chemistry  
1/28/1988 001Chemistry  
12/16/1986 000Approval  
 
Therapeutic Equivalents
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