{
  "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": "62175-261",
      "generic_name": "Nifedipine",
      "labeler_name": "Lannett Company, Inc.",
      "brand_name": "Nifedipine",
      "active_ingredients": [
        {
          "name": "NIFEDIPINE",
          "strength": "60 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "62175-261-37",
          "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-261-37)",
          "marketing_start_date": "20051121",
          "sample": false
        },
        {
          "package_ndc": "62175-261-46",
          "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-261-46)",
          "marketing_start_date": "20051121",
          "sample": false
        },
        {
          "package_ndc": "62175-261-55",
          "description": "300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-261-55)",
          "marketing_start_date": "20051121",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Lannett Company, Inc."
        ],
        "rxcui": [
          "1812011",
          "1812013",
          "1812015"
        ],
        "spl_set_id": [
          "331db003-cc8e-4509-9415-20e48c5cc5b2"
        ],
        "is_original_packager": [
          true
        ],
        "nui": [
          "N0000000069",
          "N0000175421",
          "M0006414"
        ],
        "pharm_class_moa": [
          "Calcium Channel Antagonists [MoA]"
        ],
        "pharm_class_epc": [
          "Dihydropyridine Calcium Channel Blocker [EPC]"
        ],
        "pharm_class_cs": [
          "Dihydropyridines [CS]"
        ],
        "unii": [
          "I9ZF7L6G2L"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
      "spl_id": "2b91b384-4c20-4162-a717-9dc53ea834cc",
      "product_type": "HUMAN PRESCRIPTION DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20051121",
      "product_id": "62175-261_2b91b384-4c20-4162-a717-9dc53ea834cc",
      "application_number": "ANDA077127",
      "brand_name_base": "Nifedipine",
      "pharm_class": [
        "Calcium Channel Antagonists [MoA]",
        "Dihydropyridine Calcium Channel Blocker [EPC]",
        "Dihydropyridines [CS]"
      ]
    }
  ]
}