Visitor Monitoring Drug Details: INFLAMASE FORTE
 
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Drug Details

Drug Name: INFLAMASE FORTE
FDA Application No: (ANDA) 080751
Active Ingredient(s): PREDNISOLONE SODIUM PHOSPHATE
Company: NOVARTIS
Original Approval or Tentative Approval Date: December 19, 1973
 
 
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
INFLAMASE FORTE PREDNISOLONE SODIUM PHOSPHATEEQ 0.9% PHOSPHATESOLUTION/DROPS; OPHTHALMIC Discontinued No None
INFLAMASE MILD PREDNISOLONE SODIUM PHOSPHATEEQ 0.11% PHOSPHATESOLUTION/DROPS; OPHTHALMIC Discontinued No None


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