{
  "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": "71335-0182",
      "generic_name": "Bupropion Hydrochloride",
      "labeler_name": "Bryant Ranch Prepack",
      "brand_name": "Bupropion Hydrochloride",
      "active_ingredients": [
        {
          "name": "BUPROPION HYDROCHLORIDE",
          "strength": "100 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "71335-0182-1",
          "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0182-1)",
          "marketing_start_date": "20180724",
          "sample": false
        },
        {
          "package_ndc": "71335-0182-2",
          "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0182-2)",
          "marketing_start_date": "20180620",
          "sample": false
        },
        {
          "package_ndc": "71335-0182-3",
          "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0182-3)",
          "marketing_start_date": "20240709",
          "sample": false
        },
        {
          "package_ndc": "71335-0182-4",
          "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0182-4)",
          "marketing_start_date": "20180328",
          "sample": false
        },
        {
          "package_ndc": "71335-0182-5",
          "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0182-5)",
          "marketing_start_date": "20240709",
          "sample": false
        },
        {
          "package_ndc": "71335-0182-6",
          "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-0182-6)",
          "marketing_start_date": "20240709",
          "sample": false
        },
        {
          "package_ndc": "71335-0182-7",
          "description": "21 TABLET, FILM COATED in 1 BOTTLE (71335-0182-7)",
          "marketing_start_date": "20210428",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Bryant Ranch Prepack"
        ],
        "rxcui": [
          "993687"
        ],
        "spl_set_id": [
          "2a13267f-c47f-4791-a8f9-4bbb5c804027"
        ],
        "unii": [
          "ZG7E5POY8O"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, FILM COATED",
      "spl_id": "a3743344-f956-4c63-985a-9aaaeeaad923",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20060117",
      "product_id": "71335-0182_a3743344-f956-4c63-985a-9aaaeeaad923",
      "application_number": "ANDA076143",
      "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]"
      ]
    }
  ]
}