Package 47335-061-86

{"route": ["ORAL"], "spl_id": "3ea6a12b-26de-4858-aebe-4f8902cc560f", "openfda": {"nui": ["N0000175426"], "upc": ["0347335062861", "0347335061864"], "unii": ["R4Z9X1N2ND"], "rxcui": ["310003", "310004", "310005"], "spl_set_id": ["e6caaf44-4a3e-46ef-85fa-f97f682fbdd6"], "pharm_class_epc": ["Antiarrhythmic [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (47335-061-79)  / 10 CAPSULE in 1 BLISTER PACK (47335-061-66)", "package_ndc": "47335-061-79", "marketing_start_date": "20181011"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (47335-061-86)", "package_ndc": "47335-061-86", "marketing_start_date": "20181011"}], "brand_name": "DOFETILIDE", "product_id": "47335-061_3ea6a12b-26de-4858-aebe-4f8902cc560f", "dosage_form": "CAPSULE", "pharm_class": ["Antiarrhythmic [EPC]"], "product_ndc": "47335-061", "generic_name": "DOFETILIDE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DOFETILIDE", "active_ingredients": [{"name": "DOFETILIDE", "strength": ".125 mg/1"}], "application_number": "ANDA210466", "marketing_category": "ANDA", "marketing_start_date": "20181011", "listing_expiration_date": "20261231"}