{
  "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": "68462-271",
      "generic_name": "atomoxetine",
      "labeler_name": "Glenmark Pharmaceuticals Inc., USA",
      "brand_name": "atomoxetine",
      "active_ingredients": [
        {
          "name": "ATOMOXETINE HYDROCHLORIDE",
          "strength": "100 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "68462-271-30",
          "description": "30 CAPSULE in 1 BOTTLE (68462-271-30)",
          "marketing_start_date": "20170530",
          "sample": false
        },
        {
          "package_ndc": "68462-271-51",
          "description": "1500 CAPSULE in 1 BOTTLE (68462-271-51)",
          "marketing_start_date": "20170530",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "Glenmark Pharmaceuticals Inc., USA"
        ],
        "rxcui": [
          "349591",
          "349592",
          "349593",
          "349594",
          "349595",
          "608139",
          "608143"
        ],
        "spl_set_id": [
          "0ab8d905-e890-4e91-a730-3e5d12f5c23f"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0368462265307",
          "0368462270301",
          "0368462267301",
          "0368462271308",
          "0368462268308",
          "0368462269305",
          "0368462266304"
        ],
        "unii": [
          "57WVB6I2W0"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "CAPSULE",
      "spl_id": "26737ed3-c979-48ee-b5b3-843939c09ff4",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20170530",
      "product_id": "68462-271_26737ed3-c979-48ee-b5b3-843939c09ff4",
      "application_number": "ANDA079019",
      "brand_name_base": "atomoxetine",
      "pharm_class": [
        "Norepinephrine Reuptake Inhibitor [EPC]",
        "Norepinephrine Uptake Inhibitors [MoA]"
      ]
    }
  ]
}