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United States · US · US:11673-767_46534182-fd58-f797-e063-6294a90a5106
Fexofenadine HCL
Orange BookUNIISPLATC R06AX26
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTARGET CORPORATION
CountryUS (United States)
ATC codeR06AX26
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc11116737670330 TABLET in 1 BOTTLE (11673-767-03)
- ndc11116737670715 TABLET in 1 BLISTER PACK (11673-767-07)
- ndc111167376715150 TABLET in 1 BOTTLE (11673-767-15)
- ndc11116737673470 TABLET in 1 BOTTLE (11673-767-34)
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": {
"52d50976-e63a-b3e3-e063-6294a90a6a97": {
"match": "brand_token",
"title": "FEXOFENADINE HCL TABLET [YYBA CORP]",
"spl_version": "1",
"published_date": "2026-06-01"
}
},
"productid": "11673-767_46534182-fd58-f797-e063-6294a90a5106",
"productndc": "11673-767",
"dosage_form": "TABLET",
"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": "Fexofenadine HCL",
"active_ingred_unit": "mg/1",
"application_number": "ANDA211075",
"marketing_category": "ANDA",
"nonproprietary_name": "Fexofenadine HCL",
"start_marketing_date": "20240301",
"active_numerator_strength": "180"
}Related drugs
Other records sharing ATC code R06AX26.
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