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United States · US · US:63654-415_928e4434-6c15-4bf1-bcfd-1f56a17510ed

XL - 3 Allergy

Orange BookUNIISPLATC R06AX13

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerSelder, S.A. de C.V.
CountryUS (United States)
ATC codeR06AX13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6365441510
    1 BLISTER PACK in 1 CARTON (63654-415-10) / 10 TABLET in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A210722
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "7AJO3BO7QN",
    "rxcui": "28889",
    "inchikey": "JCCNYMKQOSZNPW-UHFFFAOYSA-N",
    "display_name": "LORATADINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "059a6e72-888e-4cb3-8722-4c3acbd6b4b0": {
      "match": "brand_token",
      "title": "XL - 3 ALLERGY TABLET [SELDER, S.A. DE C.V.]",
      "spl_version": "1",
      "published_date": "2024-04-12"
    }
  },
  "productid": "63654-415_928e4434-6c15-4bf1-bcfd-1f56a17510ed",
  "productndc": "63654-415",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "210722",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Dec 23, 2019"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LORATADINE",
  "proprietary_name": "XL - 3 Allergy",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA210722",
  "marketing_category": "ANDA",
  "nonproprietary_name": "XL - 3 Allergy",
  "start_marketing_date": "20240410",
  "active_numerator_strength": "10"
}

Related drugs

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