{
  "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": "2026-10-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "49252-008",
      "generic_name": "duloxetine",
      "labeler_name": "Inventia Healthcare Limited.",
      "brand_name": "duloxetine",
      "active_ingredients": [
        {
          "name": "DULOXETINE HYDROCHLORIDE",
          "strength": "30 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "49252-008-10",
          "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-008-10)",
          "marketing_start_date": "20151205",
          "sample": false
        },
        {
          "package_ndc": "49252-008-11",
          "description": "60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-008-11)",
          "marketing_start_date": "20151205",
          "sample": false
        },
        {
          "package_ndc": "49252-008-12",
          "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-008-12)",
          "marketing_start_date": "20151205",
          "sample": false
        },
        {
          "package_ndc": "49252-008-18",
          "description": "1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49252-008-18)",
          "marketing_start_date": "20151205",
          "sample": false
        },
        {
          "package_ndc": "49252-008-57",
          "description": "100 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (49252-008-57)",
          "marketing_start_date": "20151205",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Inventia Healthcare Limited."
        ],
        "rxcui": [
          "596926",
          "596930",
          "596934"
        ],
        "spl_set_id": [
          "eab90059-ea1c-46c1-884d-c15e7c562a01"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0349252007574",
          "0349252009103",
          "0349252008106",
          "0349252008571",
          "0349252009578"
        ],
        "unii": [
          "9044SC542W"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "CAPSULE, DELAYED RELEASE",
      "spl_id": "3fb45d3e-3fbc-8814-e063-6294a90a4a70",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20151205",
      "product_id": "49252-008_3fb45d3e-3fbc-8814-e063-6294a90a4a70",
      "application_number": "ANDA202336",
      "brand_name_base": "duloxetine",
      "pharm_class": [
        "Norepinephrine Uptake Inhibitors [MoA]",
        "Serotonin Uptake Inhibitors [MoA]",
        "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"
      ]
    }
  ]
}