Visitor Monitoring Drug Details: NEO-CORTEF
 
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Drug Details

Drug Name: NEO-CORTEF
FDA Application No: (ANDA) 060751
Active Ingredient(s): HYDROCORTISONE ACETATE; NEOMYCIN SULFATE
Company: PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date: May 18, 1965
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
NEO-CORTEF HYDROCORTISONE ACETATE; NEOMYCIN SULFATE0.5%; EQ 3.5MG BASE/GMOINTMENT; TOPICAL Discontinued No None
NEO-CORTEF HYDROCORTISONE ACETATE; NEOMYCIN SULFATE1%; EQ 3.5MG BASE/GMOINTMENT; TOPICAL Discontinued No None
NEO-CORTEF HYDROCORTISONE ACETATE; NEOMYCIN SULFATE2.5%; EQ 3.5MG BASE/GMOINTMENT; TOPICAL Discontinued No None


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