🇺🇸
United States · US · US:0363-0858_a69e70f5-0044-4834-b033-571f9c36caad
Indoor Outdoor Allergy Relief
Orange BookUNIISPLATC R06AX13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerWalgreens
CountryUS (United States)
ATC codeR06AX13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 9
- ndc1103630858031 BOTTLE, PLASTIC in 1 BOX (0363-0858-03) / 30 TABLET in 1 BOTTLE, PLASTIC
- ndc1103630858055 BLISTER PACK in 1 CARTON (0363-0858-05) / 1 TABLET in 1 BLISTER PACK
- ndc11036308581010 BLISTER PACK in 1 CARTON (0363-0858-10) / 1 TABLET in 1 BLISTER PACK
- ndc1103630858151 BOTTLE, PLASTIC in 1 CARTON (0363-0858-15) / 150 TABLET in 1 BOTTLE, PLASTIC
- ndc11036308582020 BLISTER PACK in 1 CARTON (0363-0858-20) / 1 TABLET in 1 BLISTER PACK
- ndc1103630858301 BOTTLE, PLASTIC in 1 BOX (0363-0858-30) / 300 TABLET in 1 BOTTLE, PLASTIC
- ndc1103630858451 BOTTLE, PLASTIC in 1 BOX (0363-0858-45) / 45 TABLET in 1 BOTTLE, PLASTIC
- ndc1103630858701 BOTTLE, PLASTIC in 1 BOX (0363-0858-70) / 70 TABLET in 1 BOTTLE, PLASTIC
- ndc1103630858901 BOTTLE, PLASTIC in 1 BOX (0363-0858-90) / 90 TABLET in 1 BOTTLE, PLASTIC
Annotations
UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A075209
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": {
"2a94d25c-aacf-4f5c-b406-815f0e1d0611": {
"match": "brand_token",
"title": "INDOOR AND OUTDOOR ALLERGY RELIEF (CETIRIZINE HCL) TABLET, COATED [FAMORA INC.]",
"spl_version": "1",
"published_date": "2026-03-20"
}
},
"productid": "0363-0858_a69e70f5-0044-4834-b033-571f9c36caad",
"productndc": "0363-0858",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "075209",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "10MG",
"product_no": "001",
"approval_date": "Jan 21, 2003"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LORATADINE",
"proprietary_name": "Indoor Outdoor Allergy Relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA075209",
"marketing_category": "ANDA",
"nonproprietary_name": "Loratadine",
"start_marketing_date": "20180930",
"active_numerator_strength": "10"
}Related drugs
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