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



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