Visitor Monitoring Drug History: HYDROXYZINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: HYDROXYZINE HYDROCHLORIDE
FDA Application No: (ANDA) 086880
Active Ingredient(s): HYDROXYZINE HYDROCHLORIDE
Company: ACTAVIS MID ATLANTIC
 
Label History
 
Labels are not available on this site for HYDROXYZINE HYDROCHLORIDE, (ANDA) 086880
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/15/2000 032Package Change  
3/15/2000 031Manufacturing Revision  
3/15/2000 030Control Supplement  
3/15/2000 029Formulation Revision  
7/17/1998 028Chemistry  
6/12/1995 026Chemistry  
6/11/1991 025Chemistry  
9/28/1990 024Chemistry  
8/17/1992 023Chemistry  
5/9/1990 022Labeling  
5/31/1989 021Chemistry  
5/31/1989 020Chemistry  
5/31/1989 019Chemistry  
2/24/1987 018Chemistry  
2/24/1987 017Chemistry  
5/9/1986 016Chemistry  
10/2/1985 015Chemistry  
2/10/1983 013Chemistry  
3/30/1982 008Chemistry  
7/17/1980 000Approval  
 
Therapeutic Equivalents
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