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United States · US · US:73581-202_0e13664c-b422-d2fa-e063-6394a90a2d33
CETIRIZINE HYDROCHLORIDE
Orange BookUNIISPLATC R06AE
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerYYBA CORP
CountryUS (United States)
ATC codeR06AE
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc117358120201100 TABLET in 1 BOTTLE (73581-202-01)
- ndc117358120205500 TABLET in 1 BOTTLE (73581-202-05)
Annotations
UNII (FDA Substance ID)
64O047KTOA
CETIRIZINE HYDROCHLORIDE
RxCUI 203150
Orange Book
A209274
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "64O047KTOA",
"rxcui": "203150",
"inchikey": "PGLIUCLTXOYQMV-UHFFFAOYSA-N",
"display_name": "CETIRIZINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"817d07cf-5e31-421f-9e95-943bae01f5b0": {
"match": "brand_token",
"title": "CETIRIZINE HYDROCHLORIDE TABLET, CHEWABLE [SANDOZ INC]",
"spl_version": "8",
"published_date": "2026-06-01"
}
},
"productid": "73581-202_0e13664c-b422-d2fa-e063-6394a90a2d33",
"productndc": "73581-202",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "209274",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "001",
"approval_date": "Dec 22, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CETIRIZINE HYDROCHLORIDE",
"proprietary_name": "CETIRIZINE HYDROCHLORIDE",
"active_ingred_unit": "mg/1",
"application_number": "ANDA209274",
"marketing_category": "ANDA",
"nonproprietary_name": "CETIRIZINE HYDROCHLORIDE",
"start_marketing_date": "20210616",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code R06AE.
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