{
  "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": "42799-963",
      "marketing_end_date": "20270930",
      "generic_name": "venlafaxine hydrochloride, extended release",
      "labeler_name": "Edenbridge Pharmaceuticals LLC.",
      "brand_name": "venlafaxine hydrochloride, extended release",
      "active_ingredients": [
        {
          "name": "VENLAFAXINE HYDROCHLORIDE",
          "strength": "225 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "42799-963-01",
          "description": "30 TABLET in 1 BOTTLE (42799-963-01)",
          "marketing_start_date": "20230315",
          "marketing_end_date": "20270930",
          "sample": false
        },
        {
          "package_ndc": "42799-963-02",
          "description": "90 TABLET in 1 BOTTLE (42799-963-02)",
          "marketing_start_date": "20230315",
          "marketing_end_date": "20270930",
          "sample": false
        }
      ],
      "openfda": {
        "manufacturer_name": [
          "Edenbridge Pharmaceuticals LLC."
        ],
        "rxcui": [
          "808744",
          "808748"
        ],
        "spl_set_id": [
          "38431a76-6185-4c17-994f-8278b6cd7510"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "7D7RX5A8MO"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET",
      "spl_id": "157aa0f9-6266-4758-9d6b-5fc77cdc03a4",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20230315",
      "product_id": "42799-963_157aa0f9-6266-4758-9d6b-5fc77cdc03a4",
      "application_number": "ANDA209193",
      "brand_name_base": "venlafaxine hydrochloride, extended release",
      "pharm_class": [
        "Norepinephrine Uptake Inhibitors [MoA]",
        "Serotonin Uptake Inhibitors [MoA]",
        "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"
      ]
    }
  ]
}