Visitor Monitoring Drug History: MECLIZINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: MECLIZINE HYDROCHLORIDE
FDA Application No: (ANDA) 084092
Active Ingredient(s): MECLIZINE HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for MECLIZINE HYDROCHLORIDE, (ANDA) 084092
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/19/2007 106Control Supplement  
3/25/2002 100Control Supplement  
1/22/2002 099Control Supplement  
4/18/2001 098Control Supplement  
5/5/1999 097Chemistry  
2/11/1999 096Chemistry  
2/11/1999 095Chemistry  
2/11/1999 094Chemistry  
2/11/1999 093Labeling  
11/7/1995 091Chemistry  
4/23/1996 090Chemistry  
5/22/1989 087Labeling  
4/24/1986 085Chemistry  
1/28/1987 082Chemistry  
3/1/1985 080Chemistry  
3/15/1984 079Chemistry  
3/15/1984 077Chemistry  
3/15/1984 076Chemistry  
3/15/1984 075Chemistry  
3/15/1984 074Chemistry  
1/25/1984 072Chemistry  
3/11/1982 071Chemistry  
3/11/1982 070Chemistry  
3/11/1982 069Chemistry  
3/11/1982 068Chemistry  
5/13/1982 058Chemistry  
5/13/1982 057Chemistry  
5/13/1982 056Chemistry  
3/19/1975 000Approval  
 
Therapeutic Equivalents
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