Visitor Monitoring Drug Details: PREDNISOLONE SODIUM PHOSPHATE
 
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Drug Details

Drug Name: PREDNISOLONE SODIUM PHOSPHATE
FDA Application No: (ANDA) 083358
Active Ingredient(s): PREDNISOLONE SODIUM PHOSPHATE
Company: AKORN
 
Therapeutic Equivalents Labels are not available
Approval History and Related Documents are not available
 
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
PREDNISOLONE SODIUM PHOSPHATE PREDNISOLONE SODIUM PHOSPHATEEQ 0.11% PHOSPHATESOLUTION/DROPS; OPHTHALMIC Discontinued No None
PREDNISOLONE SODIUM PHOSPHATE PREDNISOLONE SODIUM PHOSPHATEEQ 0.9% PHOSPHATESOLUTION/DROPS; OPHTHALMIC Discontinued No None


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