Visitor Monitoring Drug Details: GRISACTIN
 
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Drug Details

Drug Name: GRISACTIN
FDA Application No: (NDA) 050051
Active Ingredient(s): GRISEOFULVIN, MICROCRYSTALLINE
Company: WYETH AYERST
Original Approval or Tentative Approval Date: August 22, 1962
 
There are no 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
GRISACTIN GRISEOFULVIN, MICROCRYSTALLINE250MGCAPSULE; ORAL Discontinued No None
GRISACTIN GRISEOFULVIN, MICROCRYSTALLINE125MGCAPSULE; ORAL Discontinued No None


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