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United States · US · US:11673-280_cabdfda6-5225-47a0-b627-80b4cabdaba5
up and up lansoprazole
Orange BookUNIISPLATC A02BC03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTarget Corporation
CountryUS (United States)
ATC codeA02BC03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1111673280033 BOTTLE in 1 CARTON (11673-280-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (11673-280-01)
Annotations
UNII (FDA Substance ID)
0K5C5T2QPG
LANSOPRAZOLE
RxCUI 17128
Orange Book
A202319
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "0K5C5T2QPG",
"rxcui": "17128",
"inchikey": "MJIHNNLFOKEZEW-UHFFFAOYSA-N",
"display_name": "LANSOPRAZOLE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"51c0a953-93cb-4d0a-b51c-02d9482d1746": {
"match": "brand_token",
"title": "UP AND UP ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [TARGET CORPORATION]",
"spl_version": "12",
"published_date": "2026-05-13"
}
},
"productid": "11673-280_cabdfda6-5225-47a0-b627-80b4cabdaba5",
"productndc": "11673-280",
"dosage_form": "CAPSULE, DELAYED RELEASE",
"orange_book": {
"appl_no": "202319",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "15MG",
"product_no": "001",
"approval_date": "May 18, 2012"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "LANSOPRAZOLE",
"proprietary_name": "up and up lansoprazole",
"active_ingred_unit": "mg/1",
"application_number": "ANDA202319",
"marketing_category": "ANDA",
"nonproprietary_name": "Lansoprazole",
"start_marketing_date": "20210618",
"active_numerator_strength": "15"
}Related drugs
Other records sharing ATC code A02BC03.
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