{
  "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": "2026-10-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "81968-351",
      "generic_name": "solriamfetol",
      "labeler_name": "Axsome Therapeutics, Inc.",
      "dea_schedule": "CIV",
      "brand_name": "SUNOSI",
      "active_ingredients": [
        {
          "name": "SOLRIAMFETOL",
          "strength": "150 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "81968-351-01",
          "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (81968-351-01)",
          "marketing_start_date": "20220602",
          "sample": false
        },
        {
          "package_ndc": "81968-351-07",
          "description": "7 TABLET, FILM COATED in 1 BLISTER PACK (81968-351-07)",
          "marketing_start_date": "20220602",
          "sample": true
        },
        {
          "package_ndc": "81968-351-10",
          "description": "10 BLISTER PACK in 1 CARTON (81968-351-10)  / 7 TABLET, FILM COATED in 1 BLISTER PACK (81968-351-07)",
          "marketing_start_date": "20220602",
          "sample": true
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "Axsome Therapeutics, Inc."
        ],
        "rxcui": [
          "2121756",
          "2121758",
          "2121764",
          "2173841"
        ],
        "spl_set_id": [
          "362f206b-73e7-4009-8c34-5a9df55679ab"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0381968350018",
          "0381968351015"
        ],
        "nui": [
          "N0000194049",
          "N0000000114",
          "N0000000102"
        ],
        "pharm_class_epc": [
          "Dopamine and Norepinephrine Reuptake Inhibitor [EPC]"
        ],
        "pharm_class_moa": [
          "Dopamine Uptake Inhibitors [MoA]",
          "Norepinephrine Uptake Inhibitors [MoA]"
        ],
        "unii": [
          "939U7C91AI"
        ]
      },
      "marketing_category": "NDA",
      "dosage_form": "TABLET, FILM COATED",
      "spl_id": "f0a0a507-33cd-4ab1-b438-12996fae6ae1",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20190618",
      "product_id": "81968-351_f0a0a507-33cd-4ab1-b438-12996fae6ae1",
      "application_number": "NDA211230",
      "brand_name_base": "SUNOSI",
      "pharm_class": [
        "Dopamine Uptake Inhibitors [MoA]",
        "Dopamine and Norepinephrine Reuptake Inhibitor [EPC]",
        "Norepinephrine Uptake Inhibitors [MoA]"
      ]
    }
  ]
}