{
  "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": "62756-915",
      "generic_name": "Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride",
      "labeler_name": "Sun Pharmaceutical Industries, Inc.",
      "brand_name": "Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride",
      "active_ingredients": [
        {
          "name": "CETIRIZINE HYDROCHLORIDE",
          "strength": "5 mg/1"
        },
        {
          "name": "PSEUDOEPHEDRINE HYDROCHLORIDE",
          "strength": "120 mg/1"
        }
      ],
      "finished": true,
      "packaging": [
        {
          "package_ndc": "62756-915-62",
          "description": "2 BLISTER PACK in 1 CARTON (62756-915-62)  / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (62756-915-60)",
          "marketing_start_date": "20120929",
          "sample": false
        },
        {
          "package_ndc": "62756-915-73",
          "description": "4 BLISTER PACK in 1 CARTON (62756-915-73)  / 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (62756-915-60)",
          "marketing_start_date": "20120929",
          "sample": false
        }
      ],
      "listing_expiration_date": "20261231",
      "openfda": {
        "manufacturer_name": [
          "Sun Pharmaceutical Industries, Inc."
        ],
        "rxcui": [
          "1014571"
        ],
        "spl_set_id": [
          "796c4b81-145b-4050-a851-dec81ff97006"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "64O047KTOA",
          "6V9V2RYJ8N"
        ]
      },
      "marketing_category": "ANDA",
      "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
      "spl_id": "a0bd1e9b-eb9f-46e7-8cee-10bde092d7cb",
      "product_type": "HUMAN OTC DRUG",
      "route": [
        "ORAL"
      ],
      "marketing_start_date": "20120929",
      "product_id": "62756-915_a0bd1e9b-eb9f-46e7-8cee-10bde092d7cb",
      "application_number": "ANDA090922",
      "brand_name_base": "Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride",
      "pharm_class": [
        "Adrenergic alpha-Agonists [MoA]",
        "Histamine H1 Receptor Antagonists [MoA]",
        "Histamine-1 Receptor Antagonist [EPC]",
        "alpha-Adrenergic Agonist [EPC]"
      ]
    }
  ]
}