Visitor Monitoring Drug History: MECLIZINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: MECLIZINE HYDROCHLORIDE
FDA Application No: (ANDA) 084843
Active Ingredient(s): MECLIZINE HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for MECLIZINE HYDROCHLORIDE, (ANDA) 084843
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/15/2002 098Control Supplement  
3/25/2002 097Control Supplement  
4/26/2001 096Control Supplement  
5/5/1999 095Chemistry  
3/12/1999 094Chemistry  
3/12/1999 093Chemistry  
3/12/1999 092Chemistry  
3/12/1999 091Labeling  
11/7/1995 089Chemistry  
2/7/1996 088Chemistry  
5/22/1989 085Labeling  
3/21/1986 082Chemistry  
7/5/1985 077Chemistry  
3/1/1985 076Chemistry  
4/12/1984 072Chemistry  
4/12/1984 071Chemistry  
1/25/1984 068Chemistry  
2/3/1976 000Approval  
 
Therapeutic Equivalents
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