{
  "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": "68180-560",
      "generic_name": "QUININE SULFATE",
      "labeler_name": "Lupin Pharmaceuticals, Inc.",
      "brand_name": "QUININE SULFATE",
      "active_ingredients": [
        {
          "name": "QUININE SULFATE",
          "strength": "324 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "68180-560-06",
          "description": "30 CAPSULE in 1 BOTTLE (68180-560-06)",
          "marketing_start_date": "20150804",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Lupin Pharmaceuticals, Inc."
        ],
        "rxcui": [
          "997010"
        ],
        "spl_set_id": [
          "1f32f05c-a215-40be-b951-e41a7b54a8a0"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "KF7Z0E0Q2B"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "CAPSULE",
      "spl_id": "8cd4d427-50ac-4f9c-a029-e7c2d063679a",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20150804",
      "product_id": "68180-560_8cd4d427-50ac-4f9c-a029-e7c2d063679a",
      "application_number": "ANDA203112",
      "brand_name_base": "QUININE SULFATE",
      "pharm_class": [
        "Antimalarial [EPC]"
      ]
    }
  ]
}