Visitor Monitoring Drug History: MILTOWN
 
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Label and Approval History

Drug Name: MILTOWN
FDA Application No: (NDA) 009698
Active Ingredient(s): MEPROBAMATE
Company: MEDPOINTE PHARM HLC
 
Label History
 
Labels are not available on this site for MILTOWN, (NDA) 009698
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/13/2001 036Labeling Revision  
12/13/2001 035Labeling Revision  
1/18/1994 034Formulation Revision  
8/9/1993 033Control Supplement  
3/16/1986 030Package Change  
7/1/1986 029Labeling Revision  
7/29/1981 024Manufacturing Change or Addition  
12/19/1980 023Labeling Revision  
3/10/1980 022Labeling Revision  
4/4/1979 021Manufacturing Change or Addition  
6/12/1978 020Labeling Revision  
8/26/1974 016Supplement Resubmission (MarkIV)  
1/15/1975 008Control Supplement  
4/28/1955 000Approval  
 
Therapeutic Equivalents
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