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United States · US · US:11673-753_b5be3ca8-b19c-4b5f-8018-ed6324482490
Up and Up Esomeprazole Magnesium
Orange BookUNIISPLATC A02BC05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTarget Corporation
CountryUS (United States)
ATC codeA02BC05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1111673753011 BOTTLE in 1 CARTON (11673-753-01) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
- ndc1111673753033 BOTTLE in 1 CARTON (11673-753-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
36H71644EQ
ESOMEPRAZOLE MAGNESIUM DIHYDRATE
RxCUI 1601995
Orange Book
A207193
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "36H71644EQ",
"rxcui": "1601995",
"inchikey": "DBOUSUONOXEWHU-VCKZSRROSA-N",
"display_name": "ESOMEPRAZOLE MAGNESIUM DIHYDRATE",
"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": "11673-753_b5be3ca8-b19c-4b5f-8018-ed6324482490",
"productndc": "11673-753",
"dosage_form": "CAPSULE, DELAYED RELEASE",
"orange_book": {
"appl_no": "207193",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "EQ 20MG BASE",
"product_no": "001",
"approval_date": "Aug 18, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ESOMEPRAZOLE MAGNESIUM DIHYDRATE",
"proprietary_name": "Up and Up Esomeprazole Magnesium",
"active_ingred_unit": "mg/1",
"application_number": "ANDA207193",
"marketing_category": "ANDA",
"nonproprietary_name": "esomeprazole magnesium",
"start_marketing_date": "20200313",
"active_numerator_strength": "20"
}Related drugs
Other records sharing ATC code A02BC05.
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