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United States · US · US:69230-202_09845f21-f05e-34b2-e063-6394a90a7677

Fexofenadine HCl

Orange BookUNIISPLATC R06AX26

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

Identification

ManufacturerCamber Consumer Care
CountryUS (United States)
ATC codeR06AX26
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    6923020201
    1 BOTTLE in 1 CARTON (69230-202-01) / 100 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923020205
    500 TABLET, FILM COATED in 1 BOTTLE (69230-202-05)
  • ndc11
    6923020211
    1000 TABLET, FILM COATED in 1 BOTTLE (69230-202-11)
  • ndc11
    6923020230
    1 BOTTLE in 1 CARTON (69230-202-30) / 30 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923020245
    1 BOTTLE in 1 CARTON (69230-202-45) / 45 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923020260
    1 BOTTLE in 1 CARTON (69230-202-60) / 60 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923020290
    1 BOTTLE in 1 CARTON (69230-202-90) / 90 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
2S068B75ZU
FEXOFENADINE HYDROCHLORIDE
RxCUI 236474
Orange Book
A204507
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": {
    "52d50976-e63a-b3e3-e063-6294a90a6a97": {
      "match": "brand_token",
      "title": "FEXOFENADINE HCL TABLET [YYBA CORP]",
      "spl_version": "1",
      "published_date": "2026-06-01"
    }
  },
  "productid": "69230-202_09845f21-f05e-34b2-e063-6394a90a7677",
  "productndc": "69230-202",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "204507",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "60MG",
        "product_no": "002",
        "approval_date": "Sep 16, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "180MG",
        "product_no": "003",
        "approval_date": "Sep 16, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "60MG",
        "product_no": "004",
        "approval_date": "Sep 16, 2015"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "180MG",
        "product_no": "005",
        "approval_date": "Sep 16, 2015"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FEXOFENADINE HYDROCHLORIDE",
  "proprietary_name": "Fexofenadine HCl",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA204507",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Fexofenadine HCl",
  "start_marketing_date": "20150916",
  "active_numerator_strength": "180"
}

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