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United States · US · US:69168-413_706fa553-a089-4d9b-8e40-f814a6c4dc75

Allergy Relief

Orange BookUNIISPLATC R06AX26

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

Identification

ManufacturerAllegiant Health
CountryUS (United States)
ATC codeR06AX26
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    6916841303
    3 CAPSULE, COATED in 1 CARTON (69168-413-03)
  • ndc11
    6916841306
    120 CAPSULE, COATED in 1 BOTTLE (69168-413-06)
  • ndc11
    6916841314
    250 CAPSULE, COATED in 1 BOTTLE (69168-413-14)
  • ndc11
    6916841330
    30 CAPSULE, COATED in 1 BOTTLE (69168-413-30)
  • ndc11
    6916841380
    180 CAPSULE, COATED in 1 BOTTLE (69168-413-80)
  • ndc11
    6916841382
    90 CAPSULE, COATED in 1 BOTTLE (69168-413-82)

Annotations

UNII (FDA Substance ID)
2S068B75ZU
FEXOFENADINE HYDROCHLORIDE
RxCUI 236474
Orange Book
A211075
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": "69168-413_706fa553-a089-4d9b-8e40-f814a6c4dc75",
  "productndc": "69168-413",
  "dosage_form": "CAPSULE, COATED",
  "orange_book": {
    "appl_no": "211075",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "60MG",
        "product_no": "001",
        "approval_date": "Oct 18, 2019"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "180MG",
        "product_no": "002",
        "approval_date": "Oct 18, 2019"
      }
    ],
    "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": "ANDA211075",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Fexofenadine HCl",
  "start_marketing_date": "20210322",
  "active_numerator_strength": "180"
}

Related drugs

Other records sharing ATC code R06AX26.

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