{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-09-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "63402-308",
      "generic_name": "lurasidone hydrochloride",
      "labeler_name": "Sumitomo Pharma America, Inc.",
      "brand_name": "Latuda",
      "active_ingredients": [
        {
          "name": "LURASIDONE HYDROCHLORIDE",
          "strength": "80 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "63402-308-04",
          "description": "4 BLISTER PACK in 1 CARTON (63402-308-04)  / 7 TABLET, FILM COATED in 1 BLISTER PACK (63402-308-07)",
          "marketing_start_date": "20101028",
          "sample": false
        },
        {
          "package_ndc": "63402-308-10",
          "description": "10 BLISTER PACK in 1 CARTON (63402-308-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (63402-308-01)",
          "marketing_start_date": "20101028",
          "sample": false
        },
        {
          "package_ndc": "63402-308-30",
          "description": "30 TABLET, FILM COATED in 1 BOTTLE (63402-308-30)",
          "marketing_start_date": "20101028",
          "sample": false
        },
        {
          "package_ndc": "63402-308-50",
          "description": "500 TABLET, FILM COATED in 1 BOTTLE (63402-308-50)",
          "marketing_start_date": "20101028",
          "sample": false
        },
        {
          "package_ndc": "63402-308-90",
          "description": "90 TABLET, FILM COATED in 1 BOTTLE (63402-308-90)",
          "marketing_start_date": "20101028",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "Sumitomo Pharma America, Inc."
        ],
        "rxcui": [
          "1040031",
          "1040036",
          "1040041",
          "1040043",
          "1235247",
          "1235249",
          "1297278",
          "1297357",
          "1431235",
          "1431237"
        ],
        "spl_set_id": [
          "afad3051-9df2-4c54-9684-e8262a133af8"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0363402306300",
          "0363402302302",
          "0363402304306",
          "0363402312301",
          "0363402306102",
          "0363402306508",
          "0363402308304",
          "0363402306904"
        ],
        "unii": [
          "O0P4I5851I"
        ]
      },
      "marketing_category": "NDA",
      "dosage_form": "TABLET, FILM COATED",
      "spl_id": "7383b0e0-01e8-4778-96f0-6f2e0c9586ae",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20101028",
      "product_id": "63402-308_7383b0e0-01e8-4778-96f0-6f2e0c9586ae",
      "application_number": "NDA200603",
      "brand_name_base": "Latuda",
      "pharm_class": [
        "Atypical Antipsychotic [EPC]"
      ]
    }
  ]
}