🇺🇸
United States · US · US:41250-629_1fcc8bf4-8fb6-4c59-843d-6ccbb7ae8b7e
childrens allergy relief
Orange BookUNIISPLATC R06AX13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMeijer Distribution Inc
CountryUS (United States)
ATC codeR06AX13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11412506293930 BLISTER PACK in 1 CARTON (41250-629-39) / 1 TABLET, CHEWABLE in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A210033
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": {
"436c0126-4ff3-c082-e063-6294a90a3d72": {
"match": "brand_token",
"title": "CHILDRENS IBUPROFEN (IBUPROFEN) SUSPENSION [KESIN PHARMA CORPORATION]",
"spl_version": "2",
"published_date": "2026-06-01"
}
},
"productid": "41250-629_1fcc8bf4-8fb6-4c59-843d-6ccbb7ae8b7e",
"productndc": "41250-629",
"dosage_form": "TABLET, CHEWABLE",
"orange_book": {
"appl_no": "210033",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "5MG",
"product_no": "001",
"approval_date": "Jun 12, 2019"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LORATADINE",
"proprietary_name": "childrens allergy relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA210033",
"marketing_category": "ANDA",
"nonproprietary_name": "loratadine",
"start_marketing_date": "20190827",
"active_numerator_strength": "5"
}Related drugs
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