FDA Drug Application (017469) for OMNIPRED by ALCON

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Application Number017469
Product Number001
FormSUSPENSION/DROPS;OPHTHALMIC
Dosage1%
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameOMNIPRED
Active IngredientPREDNISOLONE ACETATE

Active IngredientCount
List of drugs with Active Ingredient PREDNISOLONE ACETATE21


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