{
  "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": "71209-082",
      "generic_name": "Raloxifene hydrochloride",
      "labeler_name": "Cadila Pharmaceuticals Limited",
      "brand_name": "Raloxifene hydrochloride",
      "active_ingredients": [
        {
          "name": "RALOXIFENE HYDROCHLORIDE",
          "strength": "60 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "71209-082-01",
          "description": "30 TABLET, COATED in 1 BOTTLE (71209-082-01)",
          "marketing_start_date": "20171230",
          "sample": false
        },
        {
          "package_ndc": "71209-082-05",
          "description": "100 TABLET, COATED in 1 BOTTLE (71209-082-05)",
          "marketing_start_date": "20171230",
          "sample": false
        },
        {
          "package_ndc": "71209-082-11",
          "description": "1000 TABLET, COATED in 1 BOTTLE (71209-082-11)",
          "marketing_start_date": "20211213",
          "sample": false
        },
        {
          "package_ndc": "71209-082-13",
          "description": "2000 TABLET, COATED in 1 BOTTLE (71209-082-13)",
          "marketing_start_date": "20171230",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Cadila Pharmaceuticals Limited"
        ],
        "rxcui": [
          "1490065"
        ],
        "spl_set_id": [
          "a46bcc4f-f63d-4200-836d-a653a3c616db"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0371209082112"
        ],
        "unii": [
          "4F86W47BR6"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, COATED",
      "spl_id": "14d4c334-b49d-4479-a91e-20b7276b4eca",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20171230",
      "product_id": "71209-082_14d4c334-b49d-4479-a91e-20b7276b4eca",
      "application_number": "ANDA211324",
      "brand_name_base": "Raloxifene hydrochloride",
      "pharm_class": [
        "Estrogen Agonist/Antagonist [EPC]",
        "Selective Estrogen Receptor Modulators [MoA]"
      ]
    }
  ]
}