Allegra Allergy

Orange BookUNIISPLATC R06AX26

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

Identification

ManufacturerChattem, Inc.

CountryUS (United States)

ATC codeR06AX26

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 5

ndc11
4116741200
1 BLISTER PACK in 1 CARTON (41167-4120-0) / 5 TABLET, FILM COATED in 1 BLISTER PACK
ndc11
4116741202
3 BLISTER PACK in 1 CARTON (41167-4120-2) / 5 TABLET, FILM COATED in 1 BLISTER PACK
ndc11
4116741203
1 BOTTLE, PLASTIC in 1 CARTON (41167-4120-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
ndc11
4116741204
1 BOTTLE, PLASTIC in 1 CARTON (41167-4120-4) / 45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
ndc11
4116741206
1 BOTTLE, PLASTIC in 1 CARTON (41167-4120-6) / 70 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": "41167-4120_fb8ea8ca-b8a9-46af-9c21-d2df1100e9ff",
  "productndc": "41167-4120",
  "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        "strength": "30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",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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