🇺🇸
United States · US · US:69842-242_434285f9-116c-458e-a598-fcdcd7be2825
Loratadine
Orange BookUNIISPLATC R06AX13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCVS Pharmacy, Inc.
CountryUS (United States)
ATC codeR06AX13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 10
- ndc1169842242093 BLISTER PACK in 1 CARTON (69842-242-09) / 10 TABLET in 1 BLISTER PACK
- ndc1169842242171 BOTTLE in 1 CARTON (69842-242-17) / 45 TABLET in 1 BOTTLE
- ndc1169842242191 BOTTLE in 1 CARTON (69842-242-19) / 90 TABLET in 1 BOTTLE
- ndc116984224239365 TABLET in 1 BOTTLE (69842-242-39)
- ndc1169842242452 BOTTLE in 1 CARTON (69842-242-45) / 120 TABLET in 1 BOTTLE
- ndc1169842242541 BOTTLE in 1 CARTON (69842-242-54) / 70 TABLET in 1 BOTTLE
- ndc1169842242601 BLISTER PACK in 1 CARTON (69842-242-60) / 5 TABLET in 1 BLISTER PACK
- ndc1169842242672 BLISTER PACK in 1 CARTON (69842-242-67) / 10 TABLET in 1 BLISTER PACK
- ndc1169842242831 BLISTER PACK in 1 CARTON (69842-242-83) / 10 TABLET in 1 BLISTER PACK
- ndc1169842242913 BLISTER PACK in 1 CARTON (69842-242-91) / 10 TABLET in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A208314
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": "69842-242_434285f9-116c-458e-a598-fcdcd7be2825",
"productndc": "69842-242",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "208314",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "001",
"approval_date": "Apr 16, 2018"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LORATADINE",
"proprietary_name": "Loratadine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA208314",
"marketing_category": "ANDA",
"nonproprietary_name": "Loratadine",
"start_marketing_date": "20190826",
"active_numerator_strength": "10"
}Related drugs
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