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United States · US · US:66715-8815_031fc3e5-b5ec-447c-e063-6294a90a13b5

Non-Drowsy Allergy Relief

Orange BookUNIISPLATC R06AX13

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

Identification

ManufacturerLil' Drug Store Products, Inc.
CountryUS (United States)
ATC codeR06AX13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6671588156
    1 BLISTER PACK in 1 CARTON (66715-8815-6) / 6 TABLET in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A076471
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": {
    "3cf4b7fe-b1f7-b767-430a-655408f91753": {
      "match": "brand_token",
      "title": "NON-DROWSY ALLERGY RELIEF (FEXOFENADINE HYDROCHLORIDE) TABLET [TARGET CORPORATION]",
      "spl_version": "2",
      "published_date": "2025-08-04"
    }
  },
  "productid": "66715-8815_031fc3e5-b5ec-447c-e063-6294a90a13b5",
  "productndc": "66715-8815",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "076471",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Feb 14, 2006"
      }
    ],
    "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": "ANDA076471",
  "marketing_category": "ANDA",
  "nonproprietary_name": "loratadine tablet",
  "start_marketing_date": "20220506",
  "active_numerator_strength": "10"
}

Related drugs

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