Visitor Monitoring Drug Details: OCUSULF-10
 
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Drug Details

Drug Name: OCUSULF-10
FDA Application No: (ANDA) 080660
Active Ingredient(s): SULFACETAMIDE SODIUM
Company: MIZA PHARMS USA
Original Approval or Tentative Approval Date: August 24, 1972
 
 
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
OCUSULF-10 SULFACETAMIDE SODIUM10%SOLUTION/DROPS; OPHTHALMIC Prescription No AT
OCUSULF-30 SULFACETAMIDE SODIUM30%SOLUTION/DROPS; OPHTHALMIC Discontinued No None


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