🇺🇸
United States · US · US:73581-230_0e135981-fabe-f255-e063-6394a90ae356
LORATADINE ALLERGY RELIEF
Orange BookUNIISPLATC R06AX13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerYYBA CORP
CountryUS (United States)
ATC codeR06AX13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc117358123001100 TABLET in 1 BOTTLE (73581-230-01)
- ndc117358123036365 TABLET in 1 BOTTLE (73581-230-36)
Annotations
UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A210722
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "7AJO3BO7QN",
"rxcui": "28889",
"inchikey": "JCCNYMKQOSZNPW-UHFFFAOYSA-N",
"display_name": "LORATADINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"d778c4d2-184a-4dc8-9351-66d81d0618f2": {
"match": "brand_token",
"title": "LORATADINE TABLET [PREFERRED PHARMACEUTICALS INC.]",
"spl_version": "3",
"published_date": "2026-06-01"
}
},
"productid": "73581-230_0e135981-fabe-f255-e063-6394a90ae356",
"productndc": "73581-230",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "210722",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "001",
"approval_date": "Dec 23, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LORATADINE",
"proprietary_name": "LORATADINE ALLERGY RELIEF",
"active_ingred_unit": "mg/1",
"application_number": "ANDA210722",
"marketing_category": "ANDA",
"nonproprietary_name": "LORATADINE",
"start_marketing_date": "20220415",
"active_numerator_strength": "10"
}Related drugs
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