ibuprofen ca

Generic: ibuprofen

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

Drug Facts

Product Profile

Brand Name ibuprofen ca
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 11673-990
Product ID 11673-990_0e05da1f-2504-fd21-e063-6394a90a5ee8
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA091239
Listing Expiration 2026-12-31
Marketing Start 2020-01-01

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 11673990
Hyphenated Format 11673-990

Supplemental Identifiers

RxCUI
310965
UPC
0349483600209
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 ca (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
  • 200 TABLET, COATED in 1 BOTTLE (11673-990-20)
  • 24 TABLET, COATED in 1 BOTTLE (11673-990-42)
source: ndc

Packages (2)

11673-990-20 200 TABLET, COATED in 1 BOTTLE (11673-990-20) 11673-990-42 24 TABLET, COATED in 1 BOTTLE (11673-990-42)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

IBUPROFEN CA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0e05da1f-2504-fd21-e063-6394a90a5ee8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0349483600209"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["8e8684fa-095e-c6d6-e053-2a95a90a15b4"], "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": "200 TABLET, COATED in 1 BOTTLE (11673-990-20)", "package_ndc": "11673-990-20", "marketing_start_date": "20200101"}, {"sample": false, "description": "24 TABLET, COATED in 1 BOTTLE (11673-990-42)", "package_ndc": "11673-990-42", "marketing_start_date": "20200101"}], "brand_name": "IBUPROFEN CA", "product_id": "11673-990_0e05da1f-2504-fd21-e063-6394a90a5ee8", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-990", "generic_name": "IBUPROFEN", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN CA", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA091239", "marketing_category": "ANDA", "marketing_start_date": "20200101", "listing_expiration_date": "20261231"}