Package 63402-304-04

{"route": ["ORAL"], "spl_id": "7383b0e0-01e8-4778-96f0-6f2e0c9586ae", "openfda": {"upc": ["0363402306300", "0363402302302", "0363402304306", "0363402312301", "0363402306102", "0363402306508", "0363402308304", "0363402306904"], "unii": ["O0P4I5851I"], "rxcui": ["1040031", "1040036", "1040041", "1040043", "1235247", "1235249", "1297278", "1297357", "1431235", "1431237"], "spl_set_id": ["afad3051-9df2-4c54-9684-e8262a133af8"], "manufacturer_name": ["Sumitomo Pharma America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (63402-304-04)  / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-304-07)", "package_ndc": "63402-304-04", "marketing_start_date": "20101028"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (63402-304-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-304-01)", "package_ndc": "63402-304-10", "marketing_start_date": "20101028"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63402-304-30)", "package_ndc": "63402-304-30", "marketing_start_date": "20101028"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63402-304-50)", "package_ndc": "63402-304-50", "marketing_start_date": "20101028"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63402-304-90)", "package_ndc": "63402-304-90", "marketing_start_date": "20101028"}], "brand_name": "Latuda", "product_id": "63402-304_7383b0e0-01e8-4778-96f0-6f2e0c9586ae", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "63402-304", "generic_name": "lurasidone hydrochloride", "labeler_name": "Sumitomo Pharma America, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Latuda", "active_ingredients": [{"name": "LURASIDONE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "NDA200603", "marketing_category": "NDA", "marketing_start_date": "20101028", "listing_expiration_date": "20271231"}