up and up ibuprofen (11673-604)

Drug Facts

Product Profile

Brand Name up and up ibuprofen

Generic Name ibuprofen

Labeler target corporation

Dosage Form TABLET, FILM COATED

Routes

ORAL

Active Ingredients

ibuprofen 200 mg/1

Manufacturer

Target Corporation

Identifiers & Regulatory

Product NDC 11673-604

Product ID 11673-604_5bfbc5ad-0e3e-4469-b42f-d5ee940534cf

Product Type HUMAN OTC DRUG

Marketing Category ANDA

Application Number ANDA072096

Listing Expiration 2026-12-31

Marketing Start 2009-05-28

Pharmacologic Class

Established (EPC)

nonsteroidal anti-inflammatory drug [epc]

Mechanism of Action

cyclooxygenase inhibitors [moa]

Chemical Structure

anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673604

Hyphenated Format 11673-604

Supplemental Identifiers

RxCUI

310965

UNII

WK2XYI10QM

NUI

N0000000160 M0001335 N0000175722

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 ibuprofen (source: ndc)

Generic Name ibuprofen (source: ndc)

Application Number ANDA072096 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

200 mg/1

source: ndc

Packaging

1 BOTTLE in 1 CARTON (11673-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE
500 TABLET, FILM COATED in 1 BOTTLE (11673-604-90)

source: ndc

Packages (2)

11673-604-78 1 BOTTLE in 1 CARTON (11673-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE 11673-604-90 500 TABLET, FILM COATED in 1 BOTTLE (11673-604-90)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

up and up ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "5bfbc5ad-0e3e-4469-b42f-d5ee940534cf", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["2919fe8b-9c76-4ef6-851e-3247782cef44"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-604-78)  / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-604-78", "marketing_start_date": "20090610"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (11673-604-90)", "package_ndc": "11673-604-90", "marketing_start_date": "20150317"}], "brand_name": "up and up ibuprofen", "product_id": "11673-604_5bfbc5ad-0e3e-4469-b42f-d5ee940534cf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-604", "generic_name": "Ibuprofen", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_start_date": "20090528", "listing_expiration_date": "20261231"}