Visitor Monitoring Drug Details: METHIMAZOLE
 
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Drug Details

Drug Name: METHIMAZOLE
FDA Application No: (NDA) 040350
Active Ingredient(s): METHIMAZOLE
Company: GENPHARM
Original Approval or Tentative Approval Date: March 29, 2000
 
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
METHIMAZOLE METHIMAZOLE5MGTABLET; ORAL Prescription No AB
METHIMAZOLE METHIMAZOLE10MGTABLET; ORAL Prescription Yes AB
METHIMAZOLE METHIMAZOLE20MGTABLET; ORAL Discontinued No None


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