Visitor Monitoring Drug History: MEPROBAMATE
 
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Label and Approval History

Drug Name: MEPROBAMATE
FDA Application No: (NDA) 014882
Active Ingredient(s): MEPROBAMATE
Company: LANNETT
 
Label History
 
Labels are not available on this site for MEPROBAMATE, (NDA) 014882
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/22/1986 011Labeling Revision  
9/22/1981 009Control Supplement  
10/24/1978 008Manufacturing Change or Addition  
4/25/1978 007Labeling Revision  
9/8/1977 006Control Supplement  
9/8/1977 005Labeling Revision  
8/9/1963 000Approval  
 
Therapeutic Equivalents
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