{
  "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": "2026-10-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "71610-866",
      "generic_name": "bupropion Hydrochloride",
      "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC",
      "brand_name": "bupropion Hydrochloride",
      "active_ingredients": [
        {
          "name": "BUPROPION HYDROCHLORIDE",
          "strength": "75 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "71610-866-53",
          "description": "60 TABLET in 1 BOTTLE (71610-866-53)",
          "marketing_start_date": "20241121",
          "sample": false
        },
        {
          "package_ndc": "71610-866-60",
          "description": "90 TABLET in 1 BOTTLE (71610-866-60)",
          "marketing_start_date": "20241121",
          "sample": false
        },
        {
          "package_ndc": "71610-866-70",
          "description": "120 TABLET in 1 BOTTLE (71610-866-70)",
          "marketing_start_date": "20241121",
          "sample": false
        },
        {
          "package_ndc": "71610-866-80",
          "description": "180 TABLET in 1 BOTTLE (71610-866-80)",
          "marketing_start_date": "20241121",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Aphena Pharma Solutions - Tennessee, LLC"
        ],
        "rxcui": [
          "993691"
        ],
        "spl_set_id": [
          "d0eada89-e302-4ba3-bef0-e8c69af8206e"
        ],
        "unii": [
          "ZG7E5POY8O"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET",
      "spl_id": "d103c1fe-4d4c-48e2-8e30-494b19dd7e52",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20160819",
      "product_id": "71610-866_d103c1fe-4d4c-48e2-8e30-494b19dd7e52",
      "application_number": "ANDA206975",
      "brand_name_base": "bupropion Hydrochloride",
      "pharm_class": [
        "Aminoketone [EPC]",
        "Dopamine Uptake Inhibitors [MoA]",
        "Increased Dopamine Activity [PE]",
        "Increased Norepinephrine Activity [PE]",
        "Norepinephrine Uptake Inhibitors [MoA]"
      ]
    }
  ]
}