ALLEGRA ALLERGY

Orange BookUNIISPLATC R06AX26

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerA-S Medication Solutions

CountryUS (United States)

ATC codeR06AX26

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5009012340
1 BOTTLE, PLASTIC in 1 CARTON (50090-1234-0) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)

2S068B75ZU

FEXOFENADINE HYDROCHLORIDE

RxCUI 236474

Orange Book

N020872

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": {
    "b82d993a-16ff-4037-a182-7010de8e1cdd": {
      "match": "brand_token",
      "title": "ALLEGRA ALLERGY (FEXOFENADINE HYDROCHLORIDE) TABLET, FILM COATED ALLEGRA ALLERGY, TRAVEL BASIX (FEXOFENADINE HYDROCHLORIDE) TABLET, FILM COATED [LIL' DRUG STORE PRODUCTS, INC]",
      "spl_version": "9",
      "published_date": "2026-04-29"
    }
  },
  "productid": "50090-1234_9840fda7-e713-4573-8029-046a50c67462",
  "productndc": "50090-1234",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "020872",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
        "product_no": "005",
        "approval_date": "Jan 24, 2011"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "30MG",
        "product_no": "006",
        "approval_date": "Jan 24, 2011"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "60MG",
        "product_no": "007",
        "approval_date": "Jan 24, 2011"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "60MG",
        "product_no": "008",
        "approval_date": "Jan 24, 2011"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "180MG",
        "product_no": "009",
        "approval_date": "Jan 24, 2011"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "180MG",
        "product_no": "010",
        "approval_date": "Jan 24, 2011"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FEXOFENADINE HYDROCHLORIDE",
  "proprietary_name": "ALLEGRA ALLERGY",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA020872",
  "marketing_category": "NDA",
  "nonproprietary_name": "fexofenadine hydrochloride",
  "start_marketing_date": "20110303",
  "active_numerator_strength": "180"
}

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