Visitor Monitoring Drug Details: BAMATE
 
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Drug Details

Drug Name: BAMATE
FDA Application No: (ANDA) 080380
Active Ingredient(s): MEPROBAMATE
Company: ALRA
Original Approval or Tentative Approval Date: July 29, 1971
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
BAMATE MEPROBAMATE200MGTABLET; ORAL Discontinued No None
BAMATE MEPROBAMATE400MGTABLET; ORAL Discontinued No None


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