{
  "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": "51662-1239",
      "generic_name": "NALOXONE HYDROCHLORIDE",
      "labeler_name": "HF Acquisition Co. LLC, DBA HealthFirst",
      "brand_name": "NALOXONE HYDROCHLORIDE",
      "active_ingredients": [
        {
          "name": "NALOXONE HYDROCHLORIDE",
          "strength": "1 mg/mL"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "51662-1239-1",
          "description": "1 SYRINGE, PLASTIC in 1 BOX (51662-1239-1)  / 2 mL in 1 SYRINGE, PLASTIC",
          "marketing_start_date": "20180903",
          "sample": false
        },
        {
          "package_ndc": "51662-1239-3",
          "description": "10 POUCH in 1 CASE (51662-1239-3)  / 1 mL in 1 POUCH (51662-1239-2)",
          "marketing_start_date": "20201027",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "HF Acquisition Co. LLC, DBA HealthFirst"
        ],
        "rxcui": [
          "1191250"
        ],
        "spl_set_id": [
          "74fc593e-ed47-efae-e053-2991aa0a5997"
        ],
        "unii": [
          "F850569PQR"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "INJECTION",
      "spl_id": "0fcaff2c-afb8-788b-e063-6394a90ade78",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "PARENTERAL"
      ],
      "marketing_start_date": "20180903",
      "product_id": "51662-1239_0fcaff2c-afb8-788b-e063-6394a90ade78",
      "application_number": "ANDA072076",
      "brand_name_base": "NALOXONE HYDROCHLORIDE",
      "pharm_class": [
        "Opioid Antagonist [EPC]",
        "Opioid Antagonists [MoA]"
      ]
    }
  ]
}