ibuprofen

Generic: ibuprofen

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

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler target corporation
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
TARGET CORPORATION

Identifiers & Regulatory

Product NDC 11673-991
Product ID 11673-991_0e071c42-0f7e-586e-e063-6394a90a9533
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091239
Listing Expiration 2026-12-31
Marketing Start 2020-02-04

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 11673991
Hyphenated Format 11673-991

Supplemental Identifiers

RxCUI
310965
UPC
0349483601886 0349483601206 0349483991505
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 ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA091239 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (11673-991-01)
  • 50 TABLET, COATED in 1 BOTTLE (11673-991-05)
  • 200 TABLET, COATED in 1 BOTTLE (11673-991-20)
  • 500 TABLET, COATED in 1 BOTTLE (11673-991-50)
  • 1000 TABLET, COATED in 1 BOTTLE (11673-991-88)
source: ndc

Packages (5)

11673-991-01 100 TABLET, COATED in 1 BOTTLE (11673-991-01) 11673-991-05 50 TABLET, COATED in 1 BOTTLE (11673-991-05) 11673-991-20 200 TABLET, COATED in 1 BOTTLE (11673-991-20) 11673-991-50 500 TABLET, COATED in 1 BOTTLE (11673-991-50) 11673-991-88 1000 TABLET, COATED in 1 BOTTLE (11673-991-88)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

IBUPROFEN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e071c42-0f7e-586e-e063-6394a90a9533", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0349483601886", "0349483601206", "0349483991505"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["8e86ae68-7687-79d6-e053-2995a90ac274"], "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": "100 TABLET, COATED in 1 BOTTLE (11673-991-01)", "package_ndc": "11673-991-01", "marketing_start_date": "20200204"}, {"sample": false, "description": "50 TABLET, COATED in 1 BOTTLE (11673-991-05)", "package_ndc": "11673-991-05", "marketing_start_date": "20200204"}, {"sample": false, "description": "200 TABLET, COATED in 1 BOTTLE (11673-991-20)", "package_ndc": "11673-991-20", "marketing_start_date": "20200204"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (11673-991-50)", "package_ndc": "11673-991-50", "marketing_start_date": "20200204"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (11673-991-88)", "package_ndc": "11673-991-88", "marketing_start_date": "20200204"}], "brand_name": "IBUPROFEN", "product_id": "11673-991_0e071c42-0f7e-586e-e063-6394a90a9533", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-991", "generic_name": "IBUPROFEN", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA091239", "marketing_category": "ANDA", "marketing_start_date": "20200204", "listing_expiration_date": "20261231"}