{
  "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": "2026-10-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "product_ndc": "57237-176",
      "generic_name": "venlafaxine hydrochloride",
      "labeler_name": "Rising Pharma Holdings, Inc.",
      "brand_name": "venlafaxine",
      "active_ingredients": [
        {
          "name": "VENLAFAXINE HYDROCHLORIDE",
          "strength": "100 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "57237-176-01",
          "description": "100 TABLET in 1 BOTTLE (57237-176-01)",
          "marketing_start_date": "20100407",
          "sample": false
        },
        {
          "package_ndc": "57237-176-90",
          "description": "90 TABLET in 1 BOTTLE (57237-176-90)",
          "marketing_start_date": "20100407",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Rising Pharma Holdings, Inc."
        ],
        "rxcui": [
          "313580",
          "313582",
          "313584",
          "313586",
          "314277"
        ],
        "spl_set_id": [
          "20319949-ccf9-477a-a6e3-53502772deb9"
        ],
        "is_original_packager": [
          true
        ],
        "upc": [
          "0357237176900",
          "0357237172902",
          "0357237174906",
          "0357237175903",
          "0357237173909"
        ],
        "unii": [
          "7D7RX5A8MO"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET",
      "spl_id": "4da7fe70-bb28-43f2-97b6-66d130e6c72f",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20100407",
      "product_id": "57237-176_4da7fe70-bb28-43f2-97b6-66d130e6c72f",
      "application_number": "ANDA090555",
      "brand_name_base": "venlafaxine",
      "pharm_class": [
        "Norepinephrine Uptake Inhibitors [MoA]",
        "Serotonin Uptake Inhibitors [MoA]",
        "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"
      ]
    }
  ]
}