FDA Drug Application (203506) for OXYMORPHONE HYDROCHLORIDE by SUN PHARM INDS LTD

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Application Number203506
Product Number001
FormTABLET, EXTENDED RELEASE;ORAL
Dosage5MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameOXYMORPHONE HYDROCHLORIDE
Active IngredientOXYMORPHONE HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient OXYMORPHONE HYDROCHLORIDE4


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