{
  "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": "2026-09-25",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 4
    }
  },
  "results": [
    {
      "product_ndc": "51672-1381",
      "generic_name": "Clindamycin and Benzoyl Peroxide Gel",
      "labeler_name": "Sun Pharmaceutical Industries, Inc.",
      "brand_name": "Clindamycin Phosphate and Benzoyl Peroxide",
      "finished": true,
      "packaging": [
        {
          "package_ndc": "51672-1381-5",
          "description": "1 KIT in 1 CARTON (51672-1381-5)  *  7 g in 1 BOTTLE, PLASTIC (51672-1382-3)  *  28 g in 1 BOTTLE, PUMP",
          "marketing_start_date": "20200121",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Sun Pharmaceutical Industries, Inc."
        ],
        "rxcui": [
          "308694",
          "309333",
          "358917"
        ],
        "spl_set_id": [
          "bde03712-b9c7-4953-af2e-d3270ba1a917"
        ],
        "is_original_packager": [
          true
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "KIT",
      "spl_id": "39629cc1-c664-52fb-e063-6294a90a69a6",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "marketing_start_date": "20200121",
      "product_id": "51672-1381_39629cc1-c664-52fb-e063-6294a90a69a6",
      "application_number": "ANDA208776",
      "brand_name_base": "Clindamycin Phosphate and Benzoyl Peroxide"
    }
  ]
}