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United States · US · US:79481-0847_dfa09879-a814-421c-8ea8-09193bc1c09d

allergy relief

Orange BookUNIISPLATC R06AX26

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

Identification

ManufacturerMeijer, Inc.
CountryUS (United States)
ATC codeR06AX26
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    7948108470
    15 BLISTER PACK in 1 CARTON (79481-0847-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    7948108471
    1 BOTTLE in 1 CARTON (79481-0847-1) / 30 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    7948108472
    1 BOTTLE in 1 CARTON (79481-0847-2) / 45 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    7948108473
    1 BOTTLE in 1 CARTON (79481-0847-3) / 40 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    7948108474
    1 BOTTLE in 1 CARTON (79481-0847-4) / 90 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
2S068B75ZU
FEXOFENADINE HYDROCHLORIDE
RxCUI 236474
Orange Book
A212971
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "2S068B75ZU",
    "rxcui": "236474",
    "inchikey": "RRJFVPUCXDGFJB-UHFFFAOYSA-N",
    "display_name": "FEXOFENADINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "934c7b91-3cba-47f0-8efa-77216f3f15c4": {
      "match": "brand_token",
      "title": "ALLERGY RELIEF CHILDRENS (DIPHENHYDRAMINE HCL) TABLET, CHEWABLE [AMERISOURCE BERGEN]",
      "spl_version": "14",
      "published_date": "2026-06-01"
    }
  },
  "productid": "79481-0847_dfa09879-a814-421c-8ea8-09193bc1c09d",
  "productndc": "79481-0847",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "212971",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "60MG",
        "product_no": "001",
        "approval_date": "Feb 24, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "180MG",
        "product_no": "002",
        "approval_date": "Feb 24, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FEXOFENADINE HYDROCHLORIDE",
  "proprietary_name": "allergy relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA212971",
  "marketing_category": "ANDA",
  "nonproprietary_name": "fexofenadine hydrochloride",
  "start_marketing_date": "20211006",
  "active_numerator_strength": "180"
}

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