{
  "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": "69097-877",
      "generic_name": "Bupropion Hydrochloride",
      "labeler_name": "Cipla USA Inc.,",
      "brand_name": "BUPROPION HYDROCHLORIDE (SR)",
      "active_ingredients": [
        {
          "name": "BUPROPION HYDROCHLORIDE",
          "strength": "100 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "69097-877-02",
          "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-877-02)",
          "marketing_start_date": "20160725",
          "sample": false
        },
        {
          "package_ndc": "69097-877-03",
          "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-877-03)",
          "marketing_start_date": "20160725",
          "sample": false
        },
        {
          "package_ndc": "69097-877-07",
          "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-877-07)",
          "marketing_start_date": "20160725",
          "sample": false
        },
        {
          "package_ndc": "69097-877-12",
          "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-877-12)",
          "marketing_start_date": "20160725",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Cipla USA Inc.,"
        ],
        "rxcui": [
          "993503",
          "993518",
          "993536"
        ],
        "spl_set_id": [
          "9d2c209b-248e-4e26-9cde-fe0abe4428c1"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0369097879037",
          "0369097878030",
          "0369097877033"
        ],
        "unii": [
          "ZG7E5POY8O"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, EXTENDED RELEASE",
      "spl_id": "a9b85841-5a69-4df1-a22d-3d4cf174e9a6",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20160725",
      "product_id": "69097-877_a9b85841-5a69-4df1-a22d-3d4cf174e9a6",
      "application_number": "ANDA206674",
      "brand_name_base": "BUPROPION HYDROCHLORIDE (SR)",
      "pharm_class": [
        "Aminoketone [EPC]",
        "Dopamine Uptake Inhibitors [MoA]",
        "Increased Dopamine Activity [PE]",
        "Increased Norepinephrine Activity [PE]",
        "Norepinephrine Uptake Inhibitors [MoA]"
      ]
    }
  ]
}