Visitor Monitoring Drug Details: MEXATE
 
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Drug Details

Drug Name: MEXATE
FDA Application No: (ANDA) 086358
Active Ingredient(s): METHOTREXATE SODIUM
Company: BRISTOL
Original Approval or Tentative Approval Date: September 5, 1979
 
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
MEXATE METHOTREXATE SODIUMEQ 20MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
MEXATE METHOTREXATE SODIUMEQ 50MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
MEXATE METHOTREXATE SODIUMEQ 100MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
MEXATE METHOTREXATE SODIUMEQ 250MG BASE/VIALINJECTABLE; INJECTION Discontinued No None


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