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United States · US · US:11523-4359_4536cd82-d67c-56be-e063-6294a90a7775
Claritin
Orange BookUNIISPLATC R06AX13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBayer HealthCare LLC.
CountryUS (United States)
ATC codeR06AX13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 9
- ndc1111523435911 BOTTLE in 1 CARTON (11523-4359-1) / 40 TABLET in 1 BOTTLE
- ndc1111523435921 BOTTLE in 1 CARTON (11523-4359-2) / 100 TABLET in 1 BOTTLE
- ndc1111523435931 BOTTLE in 1 CARTON (11523-4359-3) / 90 TABLET in 1 BOTTLE
- ndc1111523435941 BOTTLE in 1 CARTON (11523-4359-4) / 55 TABLET in 1 BOTTLE
- ndc1111523435951 BOTTLE in 1 CARTON (11523-4359-5) / 85 TABLET in 1 BOTTLE
- ndc1111523435961 BOTTLE in 1 CARTON (11523-4359-6) / 110 TABLET in 1 BOTTLE
- ndc1111523435971 BOTTLE in 1 BLISTER PACK (11523-4359-7) / 115 TABLET in 1 BOTTLE
- ndc1111523435982 BOTTLE in 1 BLISTER PACK (11523-4359-8) / 60 TABLET in 1 BOTTLE
- ndc1111523435991 BOTTLE in 1 CARTON (11523-4359-9) / 35 TABLET in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
N019658
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": {
"8e14b61f-faf6-43a8-a080-75f64514217a": {
"match": "brand_token",
"title": "CLARITIN LIQUI-GELS (LORATADINE) CAPSULE, LIQUID FILLED [BAYER HEALTHCARE LLC.]",
"spl_version": "13",
"published_date": "2026-02-09"
}
},
"productid": "11523-4359_4536cd82-d67c-56be-e063-6294a90a7775",
"productndc": "11523-4359",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "019658",
"products": [
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "10MG",
"product_no": "002",
"approval_date": "Nov 27, 2002"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "10MG",
"product_no": "003",
"approval_date": "Nov 19, 2003"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LORATADINE",
"proprietary_name": "Claritin",
"active_ingred_unit": "mg/1",
"application_number": "NDA019658",
"marketing_category": "NDA",
"nonproprietary_name": "Loratadine",
"start_marketing_date": "19930412",
"active_numerator_strength": "10"
}Related drugs
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