up and up esomeprazole magnesium

Generic: esomeprazole magnesium

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name up and up esomeprazole magnesium
Generic Name esomeprazole magnesium
Labeler target corporation
Dosage Form CAPSULE, DELAYED RELEASE
Routes
ORAL
Active Ingredients

esomeprazole magnesium dihydrate 20 mg/1

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-753
Product ID 11673-753_b5be3ca8-b19c-4b5f-8018-ed6324482490
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207193
Listing Expiration 2026-12-31
Marketing Start 2020-03-13

Pharmacologic Class

Classes
cytochrome p450 2c19 inhibitors [moa] proton pump inhibitor [epc] proton pump inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673753
Hyphenated Format 11673-753

Supplemental Identifiers

RxCUI
606726
UNII
36H71644EQ

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name up and up esomeprazole magnesium (source: ndc)
Generic Name esomeprazole magnesium (source: ndc)
Application Number ANDA207193 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (11673-753-01) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
  • 3 BOTTLE in 1 CARTON (11673-753-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
source: ndc

Packages (2)

11673-753-01 1 BOTTLE in 1 CARTON (11673-753-01) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE 11673-753-03 3 BOTTLE in 1 CARTON (11673-753-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE

Ingredients (1)

esomeprazole magnesium dihydrate (20 mg/1)

Linked Drug Pages (1)

Up and Up Esomeprazole Magnesium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b5be3ca8-b19c-4b5f-8018-ed6324482490", "openfda": {"unii": ["36H71644EQ"], "rxcui": ["606726"], "spl_set_id": ["b3d3ad1d-96f8-4f72-ae66-f14940a62882"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-753-01)  / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "11673-753-01", "marketing_start_date": "20200313"}, {"sample": false, "description": "3 BOTTLE in 1 CARTON (11673-753-03)  / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "11673-753-03", "marketing_start_date": "20200313"}], "brand_name": "Up and Up Esomeprazole Magnesium", "product_id": "11673-753_b5be3ca8-b19c-4b5f-8018-ed6324482490", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "11673-753", "generic_name": "esomeprazole magnesium", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and Up Esomeprazole Magnesium", "active_ingredients": [{"name": "ESOMEPRAZOLE MAGNESIUM DIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA207193", "marketing_category": "ANDA", "marketing_start_date": "20200313", "listing_expiration_date": "20261231"}