up and up omeprazole

Generic: omeprazole

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

Drug Facts

Product Profile

Brand Name up and up omeprazole
Generic Name omeprazole
Labeler target corporation
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

omeprazole 20 mg/1

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-346
Product ID 11673-346_dc644613-1131-499d-9c16-7ee241a10c26
Product Type HUMAN OTC DRUG
Marketing Category NDA
Application Number NDA022032
Listing Expiration 2026-12-31
Marketing Start 2022-02-03

Pharmacologic Class

Established (EPC)
proton pump inhibitor [epc]
Mechanism of Action
proton pump inhibitors [moa] cytochrome p450 2c19 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673346
Hyphenated Format 11673-346

Supplemental Identifiers

RxCUI
402014
UNII
KG60484QX9
NUI
N0000175525 N0000000147 N0000182140

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 omeprazole (source: ndc)
Generic Name omeprazole (source: ndc)
Application Number NDA022032 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 3 BOTTLE in 1 CARTON (11673-346-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
source: ndc

Packages (1)

11673-346-03 3 BOTTLE in 1 CARTON (11673-346-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

Ingredients (1)

omeprazole (20 mg/1)

Linked Drug Pages (1)

up and up omeprazole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dc644613-1131-499d-9c16-7ee241a10c26", "openfda": {"nui": ["N0000175525", "N0000000147", "N0000182140"], "unii": ["KG60484QX9"], "rxcui": ["402014"], "spl_set_id": ["7dc339da-e90b-452b-b25e-8d7f3aa8bc18"], "pharm_class_epc": ["Proton Pump Inhibitor [EPC]"], "pharm_class_moa": ["Proton Pump Inhibitors [MoA]", "Cytochrome P450 2C19 Inhibitors [MoA]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BOTTLE in 1 CARTON (11673-346-03)  / 14 TABLET, DELAYED RELEASE in 1 BOTTLE", "package_ndc": "11673-346-03", "marketing_start_date": "20220203"}], "brand_name": "up and up omeprazole", "product_id": "11673-346_dc644613-1131-499d-9c16-7ee241a10c26", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Cytochrome P450 2C19 Inhibitors [MoA]", "Proton Pump Inhibitor [EPC]", "Proton Pump Inhibitors [MoA]"], "product_ndc": "11673-346", "generic_name": "omeprazole", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up omeprazole", "active_ingredients": [{"name": "OMEPRAZOLE", "strength": "20 mg/1"}], "application_number": "NDA022032", "marketing_category": "NDA", "marketing_start_date": "20220203", "listing_expiration_date": "20261231"}