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United States · US · US:41167-4320_de126d31-d1bb-490f-bf3f-fd9faf4f20ab

Allegra-D Allergy and Congestion

Orange BookUNIISPLATC R06AX

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

Identification

ManufacturerChattem, Inc.
CountryUS (United States)
ATC codeR06AX
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    4116743205
    2 BLISTER PACK in 1 CARTON (41167-4320-5) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
  • ndc11
    4116743207
    3 BLISTER PACK in 1 CARTON (41167-4320-7) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
2S068B75ZU
FEXOFENADINE HYDROCHLORIDE
RxCUI 236474
Orange Book
N021704
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": {
    "b32e172a-abf5-4c17-aa39-19e517952b91": {
      "match": "brand_token",
      "title": "ALLEGRA-D ALLERGY AND CONGESTION (FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [CHATTEM, INC.]",
      "spl_version": "37",
      "published_date": "2026-01-12"
    }
  },
  "productid": "41167-4320_de126d31-d1bb-490f-bf3f-fd9faf4f20ab",
  "productndc": "41167-4320",
  "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE",
  "orange_book": {
    "appl_no": "021704",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "180MG;240MG",
        "product_no": "002",
        "approval_date": "Jan 24, 2011"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE",
  "proprietary_name": "Allegra-D Allergy and Congestion",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "NDA021704",
  "marketing_category": "NDA",
  "nonproprietary_name": "fexofenadine hydrochloride and pseudoephedrine hydrochloride",
  "start_marketing_date": "20110303",
  "active_numerator_strength": "180; 240"
}

Related drugs

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