ibuprofen

Generic: ibuprofen

Labeler: kroger company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name ibuprofen
Generic Name ibuprofen
Labeler kroger company
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

ibuprofen 200 mg/1

Manufacturer
Kroger Company

Identifiers & Regulatory

Product NDC 41226-601
Product ID 41226-601_3f89772f-94d8-4e14-e063-6294a90a769b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M013
Listing Expiration 2026-12-31
Marketing Start 2021-04-10

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 41226601
Hyphenated Format 41226-601

Supplemental Identifiers

RxCUI
310965
UPC
0041260013010 0041260012990 0041260021718
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 M013 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (41226-601-01) / 100 TABLET, COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (41226-601-05) / 50 TABLET, COATED in 1 BOTTLE
  • 2 BOTTLE in 1 PACKAGE, COMBINATION (41226-601-10) / 500 TABLET, COATED in 1 BOTTLE (41226-601-53)
  • 200 TABLET, COATED in 1 BOTTLE (41226-601-20)
  • 250 TABLET, COATED in 1 BOTTLE (41226-601-25)
  • 1 BOTTLE in 1 CARTON (41226-601-42) / 24 TABLET, COATED in 1 BOTTLE
  • 500 TABLET, COATED in 1 BOTTLE (41226-601-53)
source: ndc

Packages (7)

Ingredients (1)

ibuprofen (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f89772f-94d8-4e14-e063-6294a90a769b", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0041260013010", "0041260012990", "0041260021718"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["bbedfc37-913d-8046-e053-2995a90af68a"], "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": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41226-601-01)  / 100 TABLET, COATED in 1 BOTTLE", "package_ndc": "41226-601-01", "marketing_start_date": "20210612"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41226-601-05)  / 50 TABLET, COATED in 1 BOTTLE", "package_ndc": "41226-601-05", "marketing_start_date": "20210612"}, {"sample": false, "description": "2 BOTTLE in 1 PACKAGE, COMBINATION (41226-601-10)  / 500 TABLET, COATED in 1 BOTTLE (41226-601-53)", "package_ndc": "41226-601-10", "marketing_start_date": "20240415"}, {"sample": false, "description": "200 TABLET, COATED in 1 BOTTLE (41226-601-20)", "package_ndc": "41226-601-20", "marketing_start_date": "20210612"}, {"sample": false, "description": "250 TABLET, COATED in 1 BOTTLE (41226-601-25)", "package_ndc": "41226-601-25", "marketing_start_date": "20210612"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41226-601-42)  / 24 TABLET, COATED in 1 BOTTLE", "package_ndc": "41226-601-42", "marketing_start_date": "20210410"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (41226-601-53)", "package_ndc": "41226-601-53", "marketing_start_date": "20240415"}], "brand_name": "IBUPROFEN", "product_id": "41226-601_3f89772f-94d8-4e14-e063-6294a90a769b", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "41226-601", "generic_name": "IBUPROFEN", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "M013", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210410", "listing_expiration_date": "20261231"}