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United States · US · US:41250-890_a567dea7-7d0e-4326-9167-e1e9c4cb8731

non drowsy allergy relief

Orange BookUNIISPLATC R06AX13

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

Identification

ManufacturerMeijer Distribution Inc
CountryUS (United States)
ATC codeR06AX13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    4125089065
    30 BLISTER PACK in 1 CARTON (41250-890-65) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A076011
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": {
    "600855d4-36c4-41d6-a7aa-d0f373aad57e": {
      "match": "brand_token",
      "title": "NON IODINE BARRIER DIP (IODINE) SOLUTION [SURPASS CHEMICAL COMPANY, INC.]",
      "spl_version": "2",
      "published_date": "2025-12-31"
    }
  },
  "productid": "41250-890_a567dea7-7d0e-4326-9167-e1e9c4cb8731",
  "productndc": "41250-890",
  "dosage_form": "TABLET, ORALLY DISINTEGRATING",
  "orange_book": {
    "appl_no": "076011",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Sep 29, 2003"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LORATADINE",
  "proprietary_name": "non drowsy allergy relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA076011",
  "marketing_category": "ANDA",
  "nonproprietary_name": "loratadine",
  "start_marketing_date": "20200923",
  "active_numerator_strength": "10"
}

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