Visitor Monitoring Drug History: CLONIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CLONIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 070974
Active Ingredient(s): CLONIDINE HYDROCHLORIDE
Company: ACTAVIS ELIZABETH
 
Label History
 
Labels are not available on this site for CLONIDINE HYDROCHLORIDE, (ANDA) 070974
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/8/2002 016Control Supplement  
11/2/2001 015Control Supplement  
3/20/2000 014Facility Addition  
3/20/2000 013Facility Addition  
2/18/1997 012Labeling  
1/18/1996 010Chemistry  
2/4/1992 009Chemistry  
10/13/1989 008Labeling  
11/21/1990 007Chemistry  
11/17/1988 006Labeling  
11/17/1988 005Labeling  
1/28/1988 004Chemistry  
6/9/1987 002Chemistry  
6/9/1987 001Chemistry  
12/16/1986 000Approval  
 
Therapeutic Equivalents
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