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United States · US · US:68210-0119_2a804c42-e22a-703e-e063-6394a90a3b1b
CABINET Allergy Relief
Orange BookUNIISPLATC R06AE
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSpirit Pharmaceutical LLC
CountryUS (United States)
ATC codeR06AE
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc116821001190100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68210-0119-0)
- ndc116821001191300 TABLET, FILM COATED in 1 BOTTLE (68210-0119-1)
- ndc1168210011931 BOTTLE, PLASTIC in 1 CARTON (68210-0119-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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": {
"5237c8bd-0b20-4639-a740-f3001c4c2c94": {
"match": "brand_token",
"title": "CABINET ALLERGY RELIEF FEXOFENADINE (FEXOFENADINE HYDROCHLORIDE) TABLET [CABINET HEALTH P.B.C.]",
"spl_version": "2",
"published_date": "2025-11-17"
}
},
"productid": "68210-0119_2a804c42-e22a-703e-e063-6394a90a3b1b",
"productndc": "68210-0119",
"dosage_form": "TABLET, FILM COATED",
"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": "CABINET Allergy Relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA209274",
"marketing_category": "ANDA",
"nonproprietary_name": "Cetirizine Hydrochloride",
"start_marketing_date": "20191025",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code R06AE.
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