🇺🇸
United States · US · US:59779-528_a6cabd7d-4312-4e21-a04d-bc8bbeafbdfb
Loratadine
Orange BookUNIISPLATC R06AX13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCVS Pharmacy
CountryUS (United States)
ATC codeR06AX13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 9
- ndc1159779528212 BLISTER PACK in 1 CARTON (59779-528-21) / 10 TABLET in 1 BLISTER PACK
- ndc1159779528313 BLISTER PACK in 1 CARTON (59779-528-31) / 10 TABLET in 1 BLISTER PACK
- ndc1159779528372 BOTTLE in 1 CARTON (59779-528-37) / 120 TABLET in 1 BOTTLE
- ndc1159779528381 BOTTLE in 1 CARTON (59779-528-38) / 365 TABLET in 1 BOTTLE
- ndc1159779528431 BOTTLE in 1 CARTON (59779-528-43) / 45 TABLET in 1 BOTTLE
- ndc1159779528561 BLISTER PACK in 1 CARTON (59779-528-56) / 5 TABLET in 1 BLISTER PACK
- ndc1159779528601 BOTTLE in 1 CARTON (59779-528-60) / 60 TABLET in 1 BOTTLE
- ndc1159779528691 BLISTER PACK in 1 CARTON (59779-528-69) / 10 TABLET in 1 BLISTER PACK
- ndc1159779528932 BOTTLE in 1 CARTON (59779-528-93) / 30 TABLET in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A076134
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": "59779-528_a6cabd7d-4312-4e21-a04d-bc8bbeafbdfb",
"productndc": "59779-528",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "076134",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "001",
"approval_date": "Aug 18, 2003"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LORATADINE",
"proprietary_name": "Loratadine",
"active_ingred_unit": "mg/1",
"application_number": "ANDA076134",
"marketing_category": "ANDA",
"nonproprietary_name": "Loratadine",
"start_marketing_date": "20100108",
"active_numerator_strength": "10"
}Related drugs
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