{
  "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": "70518-2551",
      "generic_name": "Hydralazine Hydrochloride",
      "labeler_name": "REMEDYREPACK INC.",
      "brand_name": "Hydralazine Hydrochloride",
      "active_ingredients": [
        {
          "name": "HYDRALAZINE HYDROCHLORIDE",
          "strength": "25 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "70518-2551-0",
          "description": "30 TABLET in 1 BLISTER PACK (70518-2551-0)",
          "marketing_start_date": "20200122",
          "sample": false
        },
        {
          "package_ndc": "70518-2551-1",
          "description": "30 TABLET in 1 BLISTER PACK (70518-2551-1)",
          "marketing_start_date": "20250731",
          "sample": false
        },
        {
          "package_ndc": "70518-2551-2",
          "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-2551-2)",
          "marketing_start_date": "20250904",
          "sample": false
        },
        {
          "package_ndc": "70518-2551-3",
          "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-2551-3)",
          "marketing_start_date": "20250904",
          "sample": false
        }
      ],
      "listing_expiration_date": "20271231",
      "openfda": {
        "manufacturer_name": [
          "REMEDYREPACK INC."
        ],
        "rxcui": [
          "905225"
        ],
        "spl_set_id": [
          "89afc8ef-27c4-489a-81de-3f8f65f6bbb8"
        ],
        "unii": [
          "FD171B778Y"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET",
      "spl_id": "4a67249e-ac1c-3ea4-e063-6394a90a3fc5",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20200122",
      "product_id": "70518-2551_4a67249e-ac1c-3ea4-e063-6394a90a3fc5",
      "application_number": "ANDA040901",
      "brand_name_base": "Hydralazine Hydrochloride",
      "pharm_class": [
        "Arteriolar Vasodilation [PE]",
        "Arteriolar Vasodilator [EPC]"
      ]
    }
  ]
}