FDA Drug Application (018988) for VASOCIDIN by NOVARTIS

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Application Number018988
Product Number001
FormSOLUTION/DROPS;OPHTHALMIC
DosageEQ 0.23% PHOSPHATE;10% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameVASOCIDIN
Active IngredientPREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM

Active IngredientCount
List of drugs with Active Ingredient PREDNISOLONE ACETATE21
List of drugs with Active Ingredient PREDNISOLONE SODIUM PHOSPHATE14
List of drugs with Active Ingredient SULFACETAMIDE SODIUM30


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